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QA3 Emergency Department Stretcher - with Pressure Care Mattress
EUDAMEDFDA UDIClass I (EU MDR)
Ref 21120
Identity
- Trade Name
- QA3 Emergency Department Stretcher - with Pressure Care Mattress EUDAMEDQA3 Patient Stretcher System FDA UDI
- Generic Name
- Radiographic stretcher FDA UDI
- Device Name
- QA3 Patient Trolley System EUDAMED
- Model / Reference
- 21120 EUDAMEDQA3 Emergency Stretcher FDA UDI
Identifiers
- Catalog Number
- 21120 FDA UDI
- Primary DI / UDI-DI
- 05051995000013 EUDAMEDFDA UDI
- Basic UDI-DI
- 5051995QA3SYSTEMKP EUDAMED
- FDA Product Code
- FPO FDA UDI
- EMDN Code
- Y1299 PERSONAL MOBILITY DEVICES - OTHER EUDAMED
- GMDN Term
- Radiographic stretcher FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 880.6910 FDA UDI
- Market of Registration
- Northern 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
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
QA3 Emergency Department Stretcher - with Pressure Care Mattress by Anetic Aid 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 | 5051995QA3SYSTEMKP | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Anetic Aid Ltd
- EUDAMED SRN
- GB-MF-000011932
- Authorised Representative
- EU-UK Authorised Representative Ltd XI-AR-000010192
Sources (2)
- EUDAMED 24a3c261-b4c9-403d-a5ae-2e9e741122f2 61 fields · synced Jun 18, 2026
- FDA UDI ece1cef2-95c6-434d-ae7b-01dd13e01f70 33 fields · synced May 27, 2026