Enforcement record

Business Improvement Order disclosure naming 日本マイクロポートCRM株式会社

日本マイクロポートCRM株式会社 (医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）)

This page records one action from a Japanese government disclosure, including the published name, governing law, authority, action details, and official source.

医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）Ministry of Health, Labour and WelfareGovernment disclosure7 March 2023

Action type

Business Improvement Order

Law

医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）

Authority

Ministry of Health, Labour and Welfare

Action date

7 March 2023

RegBase evidence report

Japanese public-record enforcement check

Saveable record of the published action, regulator source, source status, and review notes for internal compliance files.

Report ID: RB-EN-ENFORCEMENT-OTHER-RI-BEN-MAIK-202608041528
Generated at: 5 August 2026 at 00:28
Record URL: https://regbase.jp/en/enforcement/other-ri-ben-maikuropotocrm-20230307

1. Review Summary

Disclosure name	日本マイクロポートCRM株式会社	Corporate Number	Not stated in the disclosure
Enforcement record	1 record	Other confirmed records for this company	Outside this report's scope
Action date	7 March 2023	Authority	Ministry of Health, Labour and Welfare
Law	医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）	Action type	Business Improvement Order
Source status	Preserved public-source archive recorded

This report summarizes public Japanese government disclosure data held by RegBase. It is not a credit score, sanctions conclusion, legal opinion, or adverse-media determination. Confirm important decisions against the linked official Japanese source.

2. Published Information

Published name	日本マイクロポートCRM株式会社

3. Enforcement Record

Target name in disclosure	日本マイクロポートCRM株式会社
Authority	Ministry of Health, Labour and Welfare (厚生労働省)
Law / action type	医薬品医療機器等の品質管理及び保証に関する法律（医療機器法） / Business Improvement Order
Action / announcement date	Action: 7 March 2023 / Announcement: 10 April 2026
English summary	Voluntary recall of the medical device (patient monitoring).
Original Japanese text	医療機器の自主回収（患者モニタリング）
Official source	https://www.mhlw.go.jp/stf/newpage_31665.html
Source archive	https://kiroku.today/a/363bd54bc4hh4brh
Extraction / evidence timestamps	Extracted: 25 April 2026 at 09:22 / Evidence checked: 25 April 2026 at 09:22 / Archive captured: 12 July 2026 at 16:31

4. Business Location and Permit Details

No additional structured business-location or permit fields are recorded for this disclosure.

5. Other Confirmed Records for This Company

This report covers the single government disclosure shown on this page.

Reviewer Notes

Reviewer		Team / company
Review purpose
Additional notes

□ Official source URL or archived source was checked.
□ Corporate Number, address, or other identifiers were reviewed to avoid confusing similarly named entities.
□ This document is understood as a public-record evidence file, not a credit decision or legal opinion.

Current page: Enforcement record

This screen focuses on one disclosed action: the published name, governing law, authority, facts, source status, and review evidence.

Free report

Save the disclosure record naming 日本マイクロポートCRM株式会社

Includes the published name, regulator, governing law, source links, archive status, and reviewer note fields for internal due-diligence files.

Preserved evidence by Kiroku

Review the preserved source for 日本マイクロポートCRM株式会社

Open the preserved public source with its capture time, original artifact, available verification data, and downloadable evidence pack.

Open preserved source and evidence pack

For developers: JSON integration details

You do not need this for normal browsing. Use it only when integrating this enforcement record into an internal tool or AI workflow.

/api/v1/enforcements?company=%E6%97%A5%E6%9C%AC%E3%83%9E%E3%82%A4%E3%82%AF%E3%83%AD%E3%83%9D%E3%83%BC%E3%83%88CRM%E6%A0%AA%E5%BC%8F%E4%BC%9A%E7%A4%BE&limit=10

Open JSON Specs

Action summary

Company: 日本マイクロポートCRM株式会社Japanese only
Original: 日本マイクロポートCRM株式会社
Governing law: 医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）
医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）
Action type: Business Improvement Order
業務改善命令
Action date: 7 March 2023
Issuing authority: Ministry of Health, Labour and Welfare
厚生労働省
Industry context: 医療機器

Violation

Machine-translated summary — verify against original

Voluntary recall of the medical device (patient monitoring).

Show original Japanese text

医療機器の自主回収（患者モニタリング）

Compliance context

Medium-high

A formal order requiring business process or compliance control improvements.

Japanese regulatory disclosure under 医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）.

Ask for remediation evidence if the company is material to your compliance, finance, or customer-facing operations.

This context is an operational aid for review workflows, not a credit opinion or legal conclusion.

Evidence pack

Original Ministry of Health, Labour and Welfare source (Japanese)Open preserved source and evidence pack

Extracted at: 2026-04-25T00:22:04.743+00:00
Evidence checked: 2026-04-25T00:22:04.743+00:00
Archive captured: 2026-07-12T07:31:11.881728+00:00

Show audit JSON

{
  "record": {
    "id": "45b80d5b-7bcd-498c-8177-d58b9e1c815f",
    "url": "https://regbase.jp/en/enforcement/other-ri-ben-maikuropotocrm-20230307",
    "company_name_original": "日本マイクロポートCRM株式会社",
    "company_name_registry": null,
    "corporate_number": null,
    "law": {
      "ja": "医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）",
      "en": "医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）"
    },
    "action_type": {
      "ja": "業務改善命令",
      "en": "Business Improvement Order"
    },
    "authority": {
      "ja": "厚生労働省",
      "en": "Ministry of Health, Labour and Welfare"
    }
  },
  "entity_match": {
    "status": "unresolved",
    "confidence": 85,
    "method": "nta_strict_name_nationally_unique",
    "method_label": "nta_strict_name_nationally_unique",
    "notes": "NTA full-download lookup found a nationally unique exact registered-name candidate (日本マイクロポートＣＲＭ株式会社). No Corporate Number was present in the disclosure, so this remains a likely match."
  },
  "review": {
    "status": "unreviewed",
    "label": "Machine extracted"
  },
  "compliance_context": {
    "severity": "Medium-high",
    "actionMeaning": "A formal order requiring business process or compliance control improvements.",
    "practicalNote": "Ask for remediation evidence if the company is material to your compliance, finance, or customer-facing operations.",
    "lawContext": "Japanese regulatory disclosure under 医薬品医療機器等の品質管理及び保証に関する法律（医療機器法）."
  },
  "evidence": {
    "recordUrl": "https://regbase.jp/en/enforcement/other-ri-ben-maikuropotocrm-20230307",
    "officialSourceUrl": "https://www.mhlw.go.jp/stf/newpage_31665.html",
    "officialDocumentUrl": null,
    "archiveUrl": "https://kiroku.today/a/363bd54bc4hh4brh",
    "archivedSourceUrl": "https://www.mhlw.go.jp/stf/newpage_31665.html",
    "archiveCapturedAt": "2026-07-12T07:31:11.881728+00:00",
    "extractedAt": "2026-04-25T00:22:04.743+00:00",
    "translatedAt": "2026-05-01T07:10:16.736+00:00",
    "evidenceCheckedAt": "2026-04-25T00:22:04.743+00:00",
    "generatedAt": "2026-08-04T15:28:03.934Z"
  },
  "limitations": [
    "RegBase aggregates public Japanese government disclosures and does not provide a credit opinion.",
    "English summaries are provided for reference. The original Japanese source is authoritative.",
    "Possible or unresolved entity matches should be manually verified before use in a decision."
  ]
}

The original Japanese disclosure is the authoritative record. Use possible or unresolved matches only as leads for manual review.

Language

日本語版を見る (Japanese)

About this recordAggregated and translated from public Japanese government disclosures. The English text is for reference only — authoritative content is the linked Japanese source.