VanishPoint® 35641
by Retractable Technologies, Inc.
VanishPoint® 35641 is a Class II device made by Retractable Technologies, Inc., listed in FDA GUDID since 22 Sep 2016 (UDI-DI 00613703356406), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00613703356406 | Date22 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00613703356406
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- VanishPoint®
- Generic name
- Peripheral intravenous cannula
- Model / Ref / Catalog
- 35641
- Primary DI / UDI-DI
- 00613703356406
- FDA product code
- FOZ
- GMDN term
- Peripheral intravenous cannula
- Device class
- Class II
- Regulation number
- 880.5200
- GUDID distribution status
- In Commercial Distribution
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