Identity
- Trade Name
- DEFENDO EUDAMEDFDA UDI
- Generic Name
- Endoscope channel support kit FDA UDI
- Device Name
- Defendo Valves Kit EUDAMEDDefendo for Fuji 700, 2-piece Single Use Air Water, and Suction Kit FDA UDI
- Model / Reference
- Defendo Valves Kit EUDAMED100336 EUDAMEDDefendo Fujifilm 700 Series FDA UDI
- Description
- Defendo for Fuji 700, 2-piece Single Use Air Water, and Suction Kit FDA UDI
Identifiers
- Catalog Number
- 100336 FDA UDI
- Primary DI / UDI-DI
- 00724995228965 EUDAMEDFDA UDI
- Basic UDI-DI
- 0724995CODEFENDVLKITF8 EUDAMED
- 510(k) Number
- K232329 FDA UDI
- FDA Product Code
- ODC FDA UDIFEQ FDA UDIFDF FDA UDI
- EMDN Code
- A030499 ADMINISTRATION KITS - OTHER EUDAMED
- GMDN Term
- Endoscope channel support kit FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Defendo by Medivators Inc. — 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 | 0724995CODEFENDVLKITF8 | 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
- Medivators Inc.
- EUDAMED SRN
- US-MF-000043422
- Authorised Representative
- STERIS Ireland Ltd IE-AR-000010065
Sources (2)
- EUDAMED d5155ed1-54f0-409f-85c2-3c48664942ab 61 fields · synced Jul 30, 2026
- FDA UDI 888c41c1-953d-473b-9347-f8690a12305a 36 fields · synced May 29, 2026