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Welch Allyn Laryngoscope English MacIntosh Fiber Optic Blade
EUDAMEDFDA UDIClass I (EU MDR)
Ref 69213Model 901038
Identity
- Trade Name
- Welch Allyn Laryngoscope English MacIntosh Fiber Optic Blade EUDAMEDWelch Allyn, Inc. FDA UDI
- Generic Name
- Rigid intubation laryngoscope, reusable FDA UDI
- Device Name
- Welch Allyn English MacIntosh #3 Fiber-Optic Laryngoscope Blade; Green Standard (ISO 7376), Stainless Steel FDA UDI
- Model / Reference
- 901038 EUDAMEDFDA UDI69213 EUDAMED
- Description
- Welch Allyn English MacIntosh #3 Fiber-Optic Laryngoscope Blade; Green Standard (ISO 7376), Stainless Steel FDA UDI
Identifiers
- Catalog Number
- 69213 FDA UDI
- Primary DI / UDI-DI
- 00732094141221 EUDAMEDFDA UDI
- Basic UDI-DI
- 0732094GMN901038F7 EUDAMED
- Direct Marketing DI
- 00732094141221 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
Moist Heat or Steam Sterilization FDA UDI
Welch Allyn Laryngoscope English MacIntosh Fiber Optic Blade by Welch Allyn, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0732094GMN901038F7 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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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 26b7f17c-dbad-49b6-a9ed-e6b15bd9e9f8 61 fields · synced Oct 6, 2026
- FDA UDI f7fac331-62fe-4e3b-9649-ed9aa1d75399 35 fields · synced May 30, 2026