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Metal Max 90 Green System Laryngoscope Blade, Phillips 2
EUDAMEDFDA UDIClass I (EU MDR)
Ref MMGS90PHI2
Identity
- Trade Name
- Metal Max 90 Green System Laryngoscope Blade, Phillips 2 EUDAMEDPROACT Metal Max 90 FDA UDI
- Generic Name
- Laryngoscope blade, single-use FDA UDI
- Device Name
- Metal Max Green System Speciality Laryngoscope Blades EUDAMEDMetal Max 90 Green System Laryngoscope Blade, Phillips 2 FDA UDI
- Model / Reference
- MMGS90PHI2 EUDAMEDFDA UDI
- Description
- Metal Max 90 Green System Laryngoscope Blade, Phillips 2 FDA UDI
Identifiers
- Catalog Number
- MMGS90PHI2 FDA UDI
- Primary DI / UDI-DI
- 25056094501809 EUDAMEDFDA UDI
- Basic UDI-DI
- 50560945MMGSSPNQ EUDAMED
- Unit of Use DI
- 15056094501802 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Metal Max 90 Green System Laryngoscope Blade, Phillips 2 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 | 50560945MMGSSPNQ | 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 5989603d-a026-48f9-aba2-c57195bf8145 61 fields · synced Jun 18, 2026
- FDA UDI e1475b53-ddce-4f92-86a3-87e8afbc5cba 36 fields · synced May 30, 2026