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Welch Allyn Laryngoscope English MacIntosh Standard Blade
EUDAMEDFDA UDIClass I (EU MDR)
Ref 69244Model 901038
Identity
- Trade Name
- Welch Allyn Laryngoscope English MacIntosh Standard Blade EUDAMEDWelch Allyn, Inc. FDA UDI
- Generic Name
- Rigid intubation laryngoscope, reusable FDA UDI
- Device Name
- Welch Allyn English MacIntosh #4 Standard Laryngoscope Blade; Stainless Steel FDA UDI
- Model / Reference
- 901038 EUDAMEDFDA UDI69244 EUDAMED
- Description
- Welch Allyn English MacIntosh #4 Standard Laryngoscope Blade; Stainless Steel FDA UDI
Identifiers
- Catalog Number
- 69244 FDA UDI
- Primary DI / UDI-DI
- 00732094141146 EUDAMEDFDA UDI
- Basic UDI-DI
- 0732094GMN901038F7 EUDAMED
- Direct Marketing DI
- 00732094141146 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
Category: Laryngoscope blade, reusable
Welch Allyn Laryngoscope English MacIntosh Standard Blade by Welch Allyn, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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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 54992d82-67d4-47c5-8e8f-d291e4f03b5d 61 fields · synced Jun 18, 2026
- FDA UDI f0372908-9597-4611-b832-69065e129344 35 fields · synced May 29, 2026