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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Wheelchair brakes FDA UDI
Device Name
ASSMBL, WHL LOCK, PAIR, K1 BASIC FDA UDI
Model / Reference
WCA806990K1B FDA UDI
Description
ASSMBL, WHL LOCK, PAIR, K1 BASIC FDA UDI

Identifiers

Catalog Number
WCA806990K1B FDA UDI
Primary DI / UDI-DI
10080196470563 FDA UDI
FDA Product Code
KNN FDA UDI
GMDN Term
Wheelchair brakes FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair brakes

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair brakes.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI cd367e58-51f8-4180-a8f9-033177f9538d 35 fields · synced May 30, 2026