# Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices, Direct Marking, and Global Unique Device Identification Database Requirements for Certain Devices:  Guidance for Industry and Food and Drug Administration Staff - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/unique-device-identification-policy-regarding-compliance-dates-for-class-i-and-unclassified-devices-direct-marking-and-global-unique-device-identification-database-requirements-for-certain-devices-guidance-for-industry-and-food-and-drug-administration-staff/b467debb-ec61-46db-b572-e2edfd670361

> FDA guidance document: Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices, Direct Marking, and Global Unique Device Identification Database Requirements for Certain Devices:  Guidance for Industry and Food and Drug Administration Staff. Issue date: July 25, 2022. Get complete insights and analysis.

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## Details

- Title: Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices, Direct Marking, and Global Unique Device Identification Database Requirements for Certain Devices:  Guidance for Industry and Food and Drug Administration Staff
- Communication Type: Guidance Document
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Office URL: /offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
- Issue Date: 2022-07-25
- Last Changed: 2022-07-22
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2017-D-6841">FDA-2017-D-6841</a>

## Related Documents

- [Unique Device Identification System: Form and Content of the Unique Device Identifier (UDI):  Guidance for Industry and Food and Drug Administration Staff](https://www.globalkeysolutions.net/guidances/guidance-document/unique-device-identification-system-form-and-content-of-the-unique-device-identifier-udi-guidance-for-industry-and-food-and-drug-administration-staff/fcaa9093-e1fb-43d3-aa8d-da6dfbfc4a01)
- [FDA and Industry Actions on De Novo Classification Requests: Effect on FDA Review Clock and Goals:  Guidance for Industry and Food and Drug Administration Staff](https://www.globalkeysolutions.net/guidances/guidance-document/fda-and-industry-actions-on-de-novo-classification-requests-effect-on-fda-review-clock-and-goals-guidance-for-industry-and-food-and-drug-administration-staff/a4f96967-2fb4-48c8-954c-0608de9ddc7b)
- [Global Unique Device Identification Database (GUDID):  Guidance for Industry and Food and Drug Administration Staff](https://www.globalkeysolutions.net/guidances/guidance-document/global-unique-device-identification-database-gudid-guidance-for-industry-and-food-and-drug-administration-staff/d3c7c927-7b69-451e-b55b-44c244ddbdc9)
