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Corehip Extended
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref NT1174Ref NT1103Ref NT1167R
by Aesculap AG
Identity
- Trade Name
- COREHIP EXTENDED EUDAMEDAESCULAP FDA UDI
- Generic Name
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
- Device Name
- COREHIP instrument set EUDAMEDCOREHIP instrument Ir EUDAMEDCOREHIP EXTENDED SYSTEM RASP SIZE 7 FDA UDI
- Model / Reference
- NT1174 EUDAMEDNT1103 EUDAMEDNT1167R EUDAMEDFDA UDI
- Description
- COREHIP EXTENDED SYSTEM RASP SIZE 7 FDA UDI
Identifiers
- Catalog Number
- NT1167R FDA UDI
- Primary DI / UDI-DI
- 04046964993244 EUDAMED04046955053926 EUDAMED04046964729614 EUDAMEDFDA UDI
- Basic UDI-DI
- 4039239000002006ZN EUDAMED403923900000149835 EUDAMED
- Direct Marketing DI
- 04046964729614 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Market of Registration
- Germany 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
EUDAMEDEUDAMED
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
Corehip Extended by Aesculap AG — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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 | 4039239000002006ZN | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (4)
- EUDAMED e512a9a1-ccdc-4a1a-a72a-e5c9299cdd24 61 fields · synced Aug 2, 2026
- EUDAMED 129bbd6b-4db4-4e21-be22-b58da3672ca6 61 fields · synced May 18, 2026
- EUDAMED 2ccabaa6-24f0-4282-b6fd-588c0c0439bf 61 fields · synced May 19, 2026
- FDA UDI 611fbe80-b98c-4196-94ff-dac145935f00 35 fields · synced May 30, 2026