Millennium 72-37793011
Millennium 72-37793011 is a Class II device made by Avalign Technologies Inc., listed in FDA GUDID since 14 Nov 2023 (UDI-DI 00190776127220), 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 | Number00190776127220 | Date14 Nov 2023 | StatusListed |
Official records
- AccessGUDID record 00190776127220
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Millennium
- Generic name
- Rigid optical cystoscope
- Model / reference
- 72-37793011
- Primary DI / UDI-DI
- 00190776127220
- FDA product code
- GCJ
- GMDN term
- Rigid optical cystoscope
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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