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Welch Allyn Laryngoscope Handle

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 60715Model 901087

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn Laryngoscope Handle EUDAMED
Welch Allyn, Inc. FDA UDI
Generic Name
Rigid intubation laryngoscope, reusable FDA UDI
Device Name
Welch Allyn 2.5 V Rechargeable Power Handle for Standard Laryngoscopes, CSA-US Certified; Medium Size; Nickel-Cadmium (#72000) Battery; IEC Plug Type-B FDA UDI
Model / Reference
901087 EUDAMEDFDA UDI
60715 EUDAMED
Description
Welch Allyn 2.5 V Rechargeable Power Handle for Standard Laryngoscopes, CSA-US Certified; Medium Size; Nickel-Cadmium (#72000) Battery; IEC Plug Type-B FDA UDI

Identifiers

Catalog Number
60715 FDA UDI
Primary DI / UDI-DI
00732094142983 EUDAMEDFDA UDI
Basic UDI-DI
0732094GMN901087FL EUDAMED
Direct Marketing DI
00732094142983 EUDAMED
FDA Product Code
CCW FDA UDI
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED
GMDN Term
Rigid intubation laryngoscope, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.5540 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laryngoscope blade, reusable

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

Similar devices

Also classified as Laryngoscope blade, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Welch Allyn, Inc.
EUDAMED SRN
US-MF-000013394
Authorised Representative
Welch Allyn Limited IE-AR-000000768

Sources (2)

  • EUDAMED c4c26f13-14c4-47a6-be2d-01b077375e68 61 fields · synced Jun 18, 2026
  • FDA UDI a8f20a05-9385-4cb7-8187-372a8714a8a4 35 fields · synced May 30, 2026