Identity
- Device Name
- Bougies EUDAMED
- Model / Reference
- 58024000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- G11358024000 EUDAMED
- Basic UDI-DI
- ++G11358024000DP EUDAMED
- EMDN Code
- G010101 OESOPHAGEAL BOUGIES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
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
Bougies by Hilbro Instruments (pvt) Ltd — Class I — 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 | ++G11358024000DP | Class I | Active |
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Manufacturer
- Manufacturer
- Hilbro Instruments (pvt) Ltd
- EUDAMED SRN
- PK-MF-000023402
- Authorised Representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Sources (1)
- EUDAMED 8c66b5f0-b8e5-4265-83ac-d2840417f95d 61 fields · synced Jul 30, 2026