Identity
- Trade Name
- BioVac FDA UDI
- Generic Name
- Endoscope suction valve, single-use FDA UDI
- Device Name
- The disposable BioVac direct suction device is indicated for transendoscopic evacuation, debulking, and/or lysing of blood, retained blood clots, or fluid, such as residual stool, within the gastrointestinal tract through the biopsy/suction channel of flexible gastrointestinal endoscopes. It also provides access for endoscopic device passage and exchange, and allows for supplemental intraprocedural irrigation when desired. FDA UDI
- Model / Reference
- 00711512 FDA UDI
- Description
- The disposable BioVac direct suction device is indicated for transendoscopic evacuation, debulking, and/or lysing of blood, retained blood clots, or fluid, such as residual stool, within the gastrointestinal tract through the biopsy/suction channel of flexible gastrointestinal endoscopes. It also provides access for endoscopic device passage and exchange, and allows for supplemental intraprocedural irrigation when desired. FDA UDI
Identifiers
- Catalog Number
- 00711512 FDA UDI
- Primary DI / UDI-DI
- 00724995183790 FDA UDI
- FDA Product Code
- KQT FDA UDI
- GMDN Term
- Endoscope suction valve, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4370 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Endoscope suction valve, single-use
BioVac by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscope suction valve, single-use.
- CeroFrict — SML Med-Tech Solutions Limited · Class II
- CeroFrict — SML Med-Tech Solutions Limited · Class II
- CeroFrict — SML Med-Tech Solutions Limited · Class II
- CeroFrict — SML Med-Tech Solutions Limited · Class II
- CeroFrict — SML Med-Tech Solutions Limited · Class II
- FUJIFILM — FUJIFILM Corporation · Class II
- CeroFrict — SML Med-Tech Solutions Limited · Class II
- CeroFrict — SML Med-Tech Solutions Limited · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- US Endoscopy
Sources (1)
- FDA UDI dc128921-9ec5-494f-bd46-6827056ffa05 36 fields · synced May 29, 2026