← Back to catalogue

Welch Allyn, Inc.

FDA UDI

Class I (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Wheelchair-accessible platform scale FDA UDI
Device Name
6002 Wheelchair Scale with standard weight (lb/kg) (X), data port (X) and battery power (X) FDA UDI
Model / Reference
901109 FDA UDI
Description
6002 Wheelchair Scale with standard weight (lb/kg) (X), data port (X) and battery power (X) FDA UDI

Identifiers

Catalog Number
6002-XX-X FDA UDI
Primary DI / UDI-DI
00732094226768 FDA UDI
FDA Product Code
INF FDA UDI
GMDN Term
Wheelchair-accessible platform scale FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3940 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair-accessible platform scale

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

Similar devices

Also classified as Wheelchair-accessible platform scale.

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

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI 839d4dc4-399d-4b05-9bb7-0421a51b099e 35 fields · synced Jun 8, 2026