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Metal Max+ Combi Laryngoscope Set with Batteries, Adult Left-Handed 3
EUDAMEDFDA UDIClass I (EU MDR)
Ref MMCB100LH3
Identity
- Trade Name
- Metal Max+ Combi Laryngoscope Set with Batteries, Adult Left-Handed 3 EUDAMEDPROACT Metal Max 100 FDA UDI
- Generic Name
- Laryngoscope blade, single-use FDA UDI
- Device Name
- Metal Max+ Combi Specialty Laryngoscopes with Pre-fitted Batteries EUDAMEDMetal Max+ Combi Laryngoscope Set with Batteries, Adult Left-Handed 3 FDA UDI
- Model / Reference
- MMCB100LH3 EUDAMEDFDA UDI
- Description
- Metal Max+ Combi Laryngoscope Set with Batteries, Adult Left-Handed 3 FDA UDI
Identifiers
- Catalog Number
- MMCB100LH3 FDA UDI
- Primary DI / UDI-DI
- 25056094502295 EUDAMEDFDA UDI
- Basic UDI-DI
- 50560945MMCBSPK7 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
- Northern 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 Laryngoscope Set with Batteries, Adult Left-Handed 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 | 50560945MMCBSPK7 | 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 73a548d2-f379-4e40-9324-024c9c6e71f0 61 fields · synced Oct 6, 2026
- FDA UDI d71ef862-69c0-420b-9387-ab958713d16a 36 fields · synced May 30, 2026