Identity
- Trade Name
- MIASPAS EUDAMEDFDA UDI
- Generic Name
- Laparoscopic access cannula, reusable FDA UDI
- Device Name
- MIASPAS instrument IIa EUDAMEDSLIDING ENDO TUBE FOR USE W/TLINSTS FDA UDI
- Model / Reference
- FL079R EUDAMEDFDA UDI
- Description
- SLIDING ENDO TUBE FOR USE W/TLINSTS FDA UDI
Identifiers
- Catalog Number
- FL079R FDA UDI
- Primary DI / UDI-DI
- 04038653167142 EUDAMEDFDA UDI
- Basic UDI-DI
- 40392390000016612Q EUDAMED
- Direct Marketing DI
- 04038653167142 EUDAMED
- FDA Product Code
- GEA FDA UDI
- EMDN Code
- L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Laparoscopic access cannula, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA 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
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
Yes
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
Miaspas 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 | 40392390000016612Q | 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 (2)
- EUDAMED ad6c24f8-e9a5-4d92-b7ef-7295397d45ae 61 fields · synced Aug 1, 2026
- FDA UDI 842e5562-ab6b-4ba7-ba96-dbc24aceb60f 36 fields · synced May 30, 2026