Identity
- Trade Name
- Obturator EUDAMEDApex FDA UDI
- Generic Name
- Surgical drill guide obturator FDA UDI
- Device Name
- Obturator EUDAMEDFDA UDI
- Model / Reference
- INS-1072 EUDAMEDFDA UDI
- Description
- Obturator FDA UDI
Identifiers
- Catalog Number
- INS-1072 FDA UDI
- Primary DI / UDI-DI
- 05391529582821 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05391529582821 EUDAMED53915295828216V EUDAMED
- Direct Marketing DI
- 05391529582821 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Surgical drill guide obturator FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Market of Registration
- 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
Yes
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
Yes
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Obturator by OrthoXel DAC — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-05391529582821 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-05391529582821 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- OrthoXel DAC
- EUDAMED SRN
- IE-MF-000000574
Sources (3)
- EUDAMED 99393f95-cb07-4e29-bf31-ab5c9ba7b0a6 61 fields · synced Jul 22, 2026
- EUDAMED 39f3f84e-452f-4b14-a1db-cdd568e07b46 61 fields · synced May 18, 2026
- FDA UDI 3003295c-e9ce-40ca-b43c-16dded084b76 36 fields · synced May 30, 2026