Millennium 1-7032930M
Millennium 1-7032930M is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 9 Sep 2025 (UDI-DI 00190776410322), 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 | Number00190776410322 | Date9 Sep 2025 | StatusListed |
Official records
- AccessGUDID record 00190776410322
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Millennium
- Generic name
- Fixed-diameter cervical dilator, reusable
- Model / reference
- 1-7032930M
- Primary DI / UDI-DI
- 00190776410322
- FDA product code
- HDQ
- GMDN term
- Fixed-diameter cervical dilator, reusable
- Device class
- Class I
- Regulation number
- 884.4530
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code HDQ (Dilator, Cervical, Fixed Size).
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- Bioteque OS265BA-3 by Bioteque Taiwan Ltd.
- CERVICAL DILATOR by Gynemetrics, Inc.
- MODEL 6500 EXTRACTION IRRIGATION SYS by Cavitron Corp.