VanishPoint®

FDA UDI

Class II (US FDA UDI)

by Retractable Technologies, Inc.

Identity

Trade Name: VanishPoint® FDA UDI
Generic Name: Blood collection set, invasive FDA UDI
Device Name: 25G x 3/4" w/12" tubing VanishPoint® Blood Collection Set, Without Luer Adapter FDA UDI
Model / Reference: 24311 FDA UDI
Description: 25G x 3/4" w/12" tubing VanishPoint® Blood Collection Set, Without Luer Adapter FDA UDI

Identifiers

Catalog Number: 24311 FDA UDI
Primary DI / UDI-DI: 00613703243102 FDA UDI
FDA Product Code: JKA FDA UDI
FPA FDA UDI
GMDN Term: Blood collection set, invasive FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 862.1675 FDA UDI
880.5440 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood collection set, invasive

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Retractable Technologies, Inc.

Sources (1)

FDA UDI 7831100c-032d-4727-bf5e-45bcf2c8a7db 35 fields · synced Jun 8, 2026