Identity
- Trade Name
- CarboJet® CO2 Bone Lavage System FDA UDI
- Generic Name
- Bone cleaning gas-jet Y-piece connector FDA UDI
- Device Name
- VacuJet® Suction Tube FDA UDI
- Model / Reference
- 25-500-0242 FDA UDI
- Description
- VacuJet® Suction Tube FDA UDI
Identifiers
- Catalog Number
- 25-500-0242 FDA UDI
- Primary DI / UDI-DI
- 00818720011783 FDA UDI
- FDA Product Code
- FQH FDA UDI
- GMDN Term
- Bone cleaning gas-jet Y-piece connector FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5475 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
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
Category: Bone cleaning gas-jet Y-piece connector
CarboJet® CO2 Bone Lavage System by Kinamed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone cleaning gas-jet Y-piece connector.
- CarboJet® CO2 Bone Lavage System — Kinamed, Inc. · Class II
- CarboJet® CO2 Bone Lavage System — Kinamed, Inc. · 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 |
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Manufacturer
- Manufacturer
- Kinamed, Inc.
Sources (1)
- FDA UDI 803f93e8-c702-4c34-a434-92726e1efc9d 34 fields · synced May 30, 2026