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Sealing adapters and sealing caps
EUDAMEDFDA UDIClass I (EU MDR)
Ref 88.01Model 10000201178
Identity
- Trade Name
- RIWO FDA UDI
- Generic Name
- Laparoscopic access cannula seal, reusable FDA UDI
- Device Name
- Sealing adapters and sealing caps EUDAMEDRUBBER CAP CAP 0.8MM probe guides, with perforation 0,8mm, (up to 7Fr.), red FDA UDI
- Model / Reference
- 10000201178 EUDAMED88.01 EUDAMED8801 FDA UDI
- Description
- RUBBER CAP CAP 0.8MM probe guides, with perforation 0,8mm, (up to 7Fr.), red FDA UDI
Identifiers
- Catalog Number
- 88.01 FDA UDI
- Primary DI / UDI-DI
- 04055207038512 EUDAMEDFDA UDI
- Basic UDI-DI
- 405520727052019-0017854Q2 EUDAMED
- Unit of Use DI
- 04055207070024 EUDAMED
- FDA Product Code
- FAJ FDA UDIFBN FDA UDI
- EMDN Code
- A0799 ADAPTERS, CONNECTORS, RAMPS, STOPCOCKS, CAPS - OTHER EUDAMED
- GMDN Term
- Laparoscopic access cannula seal, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.1500 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
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
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Sealing adapters and sealing caps by Richard Wolf GmbH — 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 | 405520727052019-0017854Q2 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
- EUDAMED SRN
- DE-MF-000007048
Sources (2)
- EUDAMED 2d641764-0435-49c5-9c0d-f41dc4b5357d 61 fields · synced Jul 30, 2026
- FDA UDI 4f7e36db-5f5d-4180-a6c5-963a781891d7 36 fields · synced May 29, 2026