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Welch Allyn, Inc.

FDA UDI

Class II (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Ambulance stretcher, manual FDA UDI
Device Name
Welch Allyn Green Series LED Procedure Headlight; One White LED, 50 Lumens, 5,500° K; Rigid Headband; Power Source Not Included FDA UDI
Model / Reference
901069 FDA UDI
Description
Welch Allyn Green Series LED Procedure Headlight; One White LED, 50 Lumens, 5,500° K; Rigid Headband; Power Source Not Included FDA UDI

Identifiers

Catalog Number
49000 FDA UDI
Primary DI / UDI-DI
00732094072198 FDA UDI
FDA Product Code
FSR FDA UDI
GMDN Term
Ambulance stretcher, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4335 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ambulance stretcher, manual

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

Similar devices

Also classified as Ambulance stretcher, manual.

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 348c4cd5-bf67-4e58-a07d-515724556dbe 35 fields · synced May 30, 2026