← Back to catalogue

VanishPoint®

FDA UDI

Class II (US FDA UDI)

by Retractable Technologies, Inc.

Identity

Trade Name
VanishPoint® FDA UDI
Generic Name
Peripheral vascular catheter FDA UDI
Device Name
14G x 1 1/4" VanishPoint® IV Catheter FEP FDA UDI
Model / Reference
35741 FDA UDI
Description
14G x 1 1/4" VanishPoint® IV Catheter FEP FDA UDI

Identifiers

Catalog Number
35741 FDA UDI
Primary DI / UDI-DI
00613703357403 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral vascular catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Peripheral vascular catheter

VanishPoint® by Retractable Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 39413ab8-fc2e-42fe-9df6-526c864ddb2a 35 fields · synced Jun 8, 2026