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KC 012-5 22mm ID Ventilator Tubing with Integral Cuffs
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- KC 012-5 22mm ID Ventilator Tubing with Integral Cuffs FDA UDI
- Generic Name
- Ventilator breathing circuit, single-use FDA UDI
- Device Name
- KC 012-5 - 12" length, 22mm ID, Clear Ventilator Tubing with Integral Cuffs. For Single Patient Use. FDA UDI
- Model / Reference
- KC 012-5 FDA UDI
- Description
- KC 012-5 - 12" length, 22mm ID, Clear Ventilator Tubing with Integral Cuffs. For Single Patient Use. FDA UDI
Identifiers
- Primary DI / UDI-DI
- M996KC01250 FDA UDI
- FDA Product Code
- BZO FDA UDI
- GMDN Term
- Ventilator breathing circuit, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5975 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
No
FDA UDI
Over-the-Counter
Yes
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
Category: Ventilator breathing circuit, single-use
KC 012-5 22mm ID Ventilator Tubing with Integral Cuffs by Instrumentation Industries, Incorporated — Class I — FDA UDI — listed in FDA GUDID
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Instrumentation Industries, Incorporated
Sources (1)
- FDA UDI 96e0d4ec-1058-4826-8c64-7d71d90ae438 34 fields · synced May 30, 2026