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Metal Max+ Green System Laryngoscope Handle with Batteries, Adult
EUDAMEDFDA UDIClass I (EU MDR)
Ref MMGSHB01
Identity
- Trade Name
- Metal Max+ Green System Laryngoscope Handle with Batteries, Adult EUDAMEDPROACT Metal Max FDA UDI
- Generic Name
- Laryngoscope handle, single-use FDA UDI
- Device Name
- Metal Max+ Green System Laryngoscope Handles with Pre-fitted Batteries EUDAMEDMetal Max+ Green System Laryngoscope Handle with Batteries, Adult FDA UDI
- Model / Reference
- MMGSHB01 EUDAMEDFDA UDI
- Description
- Metal Max+ Green System Laryngoscope Handle with Batteries, Adult FDA UDI
Identifiers
- Catalog Number
- MMGSHB01 FDA UDI
- Primary DI / UDI-DI
- 25056094500437 EUDAMEDFDA UDI
- Basic UDI-DI
- 50560945MMGSHBLT EUDAMED
- Unit of Use DI
- 15056094500430 EUDAMED
- FDA Product Code
- CCW FDA UDI
- EMDN Code
- Z12021003 LARYNGOSCOPES EUDAMED
- GMDN Term
- Laryngoscope handle, 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Laryngoscope blade, reusable
Metal Max+ Green System Laryngoscope Handle with Batteries, Adult by PROACT Medical Ltd. — 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 | 50560945MMGSHBLT | 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 ca900d72-120b-4f8a-94a0-bdbefce212c4 61 fields · synced Jul 9, 2026
- FDA UDI da324130-c69e-4d2d-896c-a9d8e84f6512 36 fields · synced May 30, 2026