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Welch Allyn, Inc.

FDA UDI

Class I (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Infant scale, electronic FDA UDI
Device Name
6102 Flush-Mounted In-Floor Scale with Kg only (K), data port (X) and flush-mounted readout (F) FDA UDI
Model / Reference
901110 FDA UDI
Description
6102 Flush-Mounted In-Floor Scale with Kg only (K), data port (X) and flush-mounted readout (F) FDA UDI

Identifiers

Catalog Number
6102-KXF-B FDA UDI
Primary DI / UDI-DI
00732094226720 FDA UDI
FDA Product Code
FRW FDA UDI
GMDN Term
Infant scale, electronic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2720 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: Infant scale, electronic

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

Similar devices

Also classified as Infant scale, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI 36ece5be-6b22-4df8-8c8a-dd53f5a1c071 35 fields · synced Jun 8, 2026