Identity
- Trade Name
- Non-Sterile Single Use TW Dilatator Probe EUDAMED
- Device Name
- Non-Sterile Single Use TW Dilatator Probe EUDAMED
- Model / Reference
- BTPR1011 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +G075BTPR10110Z EUDAMED
- Basic UDI-DI
- B-+G075BTPR10110Z EUDAMED
- EMDN Code
- L03140199 SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Category: Hand-held surgical retractor, reusable
Non-Sterile Single Use TW Dilatator Probe by Beauty Teck International (Pvt) Ltd — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-+G075BTPR10110Z | Class I | Active |
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Manufacturer
- Manufacturer
- Beauty Teck International (Pvt) Ltd
- EUDAMED SRN
- PK-MF-000009604
- Authorised Representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Sources (1)
- EUDAMED 16e8a2ac-317f-4b24-87e4-f79902e473e5 61 fields · synced Jul 21, 2026