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Single Use Specimen Bag
EUDAMEDClass IIa (EU MDR)
Ref LTX-TRB-E1000 Model LTX-TRB-E50
Identity
- Device Name
- Single Use Specimen Bag EUDAMED
- Model / Reference
- LTX-TRB-E50 EUDAMEDLTX-TRB-E1000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06971062272480 EUDAMED
- Basic UDI-DI
- 697106227TRBQW EUDAMED
- EMDN Code
- G03050199 DIGESTIVE ENDOSCOPY, RETRIEVAL DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
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
Single Use Specimen Bag by Suzhou Lantex Medical Technology Company Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 697106227TRBQW | Class IIa | Active |
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Manufacturer
- Manufacturer
- Suzhou Lantex Medical Technology Company Limited
- EUDAMED SRN
- CN-MF-000039444
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED cddd0a4a-f04b-483d-9705-a3df6d4429e8 61 fields · synced Oct 5, 2026