Millennium 1-136202
Millennium 1-136202 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 1 Nov 2021 (UDI-DI 00190776170653), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00190776170653 | Date1 Nov 2021 | StatusListed |
Official records
- AccessGUDID record 00190776170653
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Millennium
- Generic name
- Suturing needle, reusable
- Model / reference
- 1-136202
- Description
- Reverdin Needle . CVD
- Primary DI / UDI-DI
- 00190776170653
- FDA product code
- GDL
- GMDN term
- Suturing needle, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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