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Metal Max+ Combi 50 Laryngoscope with Batteries, Adult Macintosh 3
EUDAMEDFDA UDIClass I (EU MDR)
Ref MMCB50MAC3
Identity
- Trade Name
- Metal Max+ Combi 50 Laryngoscope with Batteries, Adult Macintosh 3 EUDAMEDPROACT Metal Max 50 FDA UDI
- Generic Name
- Laryngoscope blade, single-use FDA UDI
- Device Name
- Metal Max+ Combi 50 Laryngoscopes with Pre-fitted Batteries EUDAMEDMetal Max+ Combi 50 Laryngoscope with Batteries, Adult Macintosh 3 FDA UDI
- Model / Reference
- MMCB50MAC3 EUDAMEDFDA UDI
- Description
- Metal Max+ Combi 50 Laryngoscope with Batteries, Adult Macintosh 3 FDA UDI
Identifiers
- Catalog Number
- MMCB50MAC3 FDA UDI
- Primary DI / UDI-DI
- 25060179638052 EUDAMEDFDA UDI
- Basic UDI-DI
- 50560945MMCB50EJ EUDAMED
- Unit of Use DI
- 15060179638055 EUDAMED
- FDA Product Code
- CCW FDA UDI
- EMDN Code
- R9002 LARYNGOSCOPE BLADES, SINGLE-USE EUDAMED
- GMDN Term
- Laryngoscope blade, single-use 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
Yes
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
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Metal Max+ Combi 50 Laryngoscope with Batteries, Adult Macintosh 3 by PROACT Medical Ltd. — 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 | 50560945MMCB50EJ | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- PROACT Medical Ltd.
- EUDAMED SRN
- GB-MF-000006294
- Authorised Representative
- Acorn Regulatory Consultancy Services Ltd IE-AR-000000592
Sources (2)
- EUDAMED 2ba13438-0d5f-48b6-b83c-f29eb616ce21 61 fields · synced Aug 2, 2026
- FDA UDI f2d4c090-502c-4835-86a3-1f949d932f8d 36 fields · synced May 30, 2026