← Back to catalogue
Collecting containers for suction pumps
EUDAMEDFDA UDIClass I (EU MDR)
Ref 2228.801Model 10000201483
Identity
- Trade Name
- NA FDA UDI
- Generic Name
- Surgical suction system collection container, reusable FDA UDI
- Device Name
- Collecting containers for suction pumps EUDAMEDCHIP COLLECTING CONTAINER for hysteroscopy, for the suction of tissue during resection, max. suction power 750mbar FDA UDI
- Model / Reference
- 10000201483 EUDAMED2228.801 EUDAMED2228801 FDA UDI
- Description
- CHIP COLLECTING CONTAINER for hysteroscopy, for the suction of tissue during resection, max. suction power 750mbar FDA UDI
Identifiers
- Catalog Number
- 2228.801 FDA UDI
- Primary DI / UDI-DI
- 04055207011911 EUDAMEDFDA UDI
- Basic UDI-DI
- 405520727052019-0028706Q4 EUDAMED
- FDA Product Code
- KQT FDA UDIHIH FDA UDIFJL FDA UDI
- EMDN Code
- Z12029099 VARIOUS INSTRUMENTS FOR ENDOSCOPY AND MINI–INVASIVE SURGERY – OTHER EUDAMED
- GMDN Term
- Surgical suction system collection container, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.4370 FDA UDI884.1690 FDA UDI876.1500 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
Collecting containers for suction pumps 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 | 405520727052019-0028706Q4 | 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
- Richard Wolf GmbH
- EUDAMED SRN
- DE-MF-000007048
Sources (2)
- EUDAMED f1f8a24b-9207-4c33-a378-56730f997e49 61 fields · synced Jul 9, 2026
- FDA UDI 09c51c0d-fba5-4e0a-a969-60985217a9b7 36 fields · synced May 25, 2026