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Wilburn Medical USA

FDA UDI

Class II (US FDA UDI)

by Canadian Hospital Specialties Limited

Identity

Trade Name
Wilburn Medical USA FDA UDI
Generic Name
Intravenous administration tubing extension set FDA UDI
Device Name
4" MINIBORE, NON-DEHP, T-PORT SET FDA UDI
Model / Reference
WUSA/0403 FDA UDI
Description
4" MINIBORE, NON-DEHP, T-PORT SET FDA UDI

Identifiers

Catalog Number
WUSA/0403 FDA UDI
Primary DI / UDI-DI
00628725004440 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Intravenous administration tubing extension set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

Yes

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

No

FDA UDI

Category: Intravenous administration tubing extension set

Wilburn Medical USA by Canadian Hospital Specialties Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous administration tubing extension set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Canadian Hospital Specialties Limited

Sources (1)

  • FDA UDI 6033b1c4-22a1-4eaa-8007-19c81233f5a0 34 fields · synced Jun 8, 2026