Identity
- Trade Name
- Challenger® Ti EUDAMEDAESCULAP FDA UDI
- Generic Name
- Open-surgery ligation clip applier FDA UDI
- Device Name
- CHALLENGER TI clip applier EUDAMEDCHALLENGER TI Clip Applier Forceps, multi-fire, (310 mm), diam. 5 mm, consisting of PL510R, PL522R, reusable, reposable, to be usedwith: PL572T FDA UDI
- Model / Reference
- PL512R EUDAMEDFDA UDI
- Description
- CHALLENGER TI Clip Applier Forceps, multi-fire, (310 mm), diam. 5 mm, consisting of PL510R, PL522R, reusable, reposable, to be usedwith: PL572T FDA UDI
Identifiers
- Catalog Number
- PL512R FDA UDI
- Primary DI / UDI-DI
- 04038653208456 EUDAMEDFDA UDI
- Basic UDI-DI
- 4039239000000324ZR EUDAMED
- FDA Product Code
- GDO FDA UDI
- EMDN Code
- H03020103 REUSABLE MULTIPLE CLIP APPLIERS FOR VIDEOSURGERY EUDAMED
- GMDN Term
- Open-surgery ligation clip applier FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 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
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
Challenger® Ti by Aesculap AG — Class I — 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 | 4039239000000324ZR | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED db310f3a-e500-4f7a-bae0-c16163c5590e 61 fields · synced Jul 30, 2026
- FDA UDI 50810e9b-30b9-40cf-8bea-a3d0946e44ee 36 fields · synced May 30, 2026