VanishPoint® 35441
by Retractable Technologies, Inc.
VanishPoint® 35441 is a Class II device made by Retractable Technologies, Inc., listed in FDA GUDID since 22 Sep 2016 (UDI-DI 00613703354402), 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 | Number00613703354402 | Date22 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00613703354402
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- VanishPoint®
- Generic name
- Peripheral intravenous cannula
- Model / Ref / Catalog
- 35441
- Primary DI / UDI-DI
- 00613703354402
- FDA product code
- FOZ
- GMDN term
- Peripheral intravenous cannula
- Device class
- Class II
- Regulation number
- 880.5200
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code FOZ (Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days).
- Medical Components IV Catheter by Medical Components, Inc.
- Comfort-Q Subcutaneous Injection Sets by B. Braun of America, Inc.
- Nu-Cath Emergency Kit by Intl. Medical Devices, Ltd.
- Bullett Peripheral Infusion Catheter by Cardio-Dynamics, Inc.
- DESERET MULTILUMEN SUBCLAVIAN JUGULAR by Parke-Davis Co.
- Deseret Angio-Guide Large Vein Cath. by Warner-Lambert Co.
- NIPRO SAFELET CATH by Pharma-Plast USA, Inc.
- Cook Five Lumen Central Venous Catheter by Cook, Inc.
- Nexiva Closed IV Catheter System with NearPort IV Access by Becton Dickinson Infusion Therapy Systems Inc.
- Angio-Set Intravenous Cath. Set by Deseret Medical, Inc.