Identity
- Trade Name
- KC 040 - 22mm ID Reusable Ventilator Tubing FDA UDI
- Generic Name
- Ventilator breathing circuit, reusable FDA UDI
- Device Name
- KC 040, 22mm ID, 40" length - Reusable Ventilator Tubing - polyester elastomer tube with silicone rubber cuffs FDA UDI
- Model / Reference
- KC 040 FDA UDI
- Description
- KC 040, 22mm ID, 40" length - Reusable Ventilator Tubing - polyester elastomer tube with silicone rubber cuffs FDA UDI
Identifiers
- Primary DI / UDI-DI
- M996KC0400 FDA UDI
- FDA Product Code
- BZO FDA UDI
- GMDN Term
- Ventilator breathing circuit, reusable 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
No
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, reusable
KC 040 - 22mm ID Reusable Ventilator Tubing by Instrumentation Industries, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Hytrel hose 13/13 (N/P) 40 — Drägerwerk AG & Co. KGaA · Class I
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 13a68243-3651-46b2-a0c7-57fbba6dcc13 34 fields · synced May 31, 2026