Identity
- Trade Name
- KC 105 Adapter FDA UDI
- Generic Name
- Straight/elbow breathing circuit connector, reusable FDA UDI
- Device Name
- Adult Adapter - 15mm ID/22mm OD x15mm ID/22mm OD. Fits components of adult ventilator circuits. Molded of polycarbonate. Reusable. FDA UDI
- Model / Reference
- KC 105 FDA UDI
- Description
- Adult Adapter - 15mm ID/22mm OD x15mm ID/22mm OD. Fits components of adult ventilator circuits. Molded of polycarbonate. Reusable. FDA UDI
Identifiers
- Catalog Number
- KC 105 FDA UDI
- Primary DI / UDI-DI
- M996KC1050 FDA UDI
- FDA Product Code
- BZA FDA UDI
- GMDN Term
- Straight/elbow breathing circuit connector, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5810 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: Straight/elbow breathing circuit connector, reusable
KC 105 Adapter by Instrumentation Industries, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Straight/elbow breathing circuit connector, reusable.
- 7000 CONNECTORS — HANS RUDOLPH, INC. · Class I
- Spiroguard Adaptor — GVS Filter Technology UK Ltd · Class IIa
- Airway Connector — VADI Medical Technology Co., Ltd. · Class IIa
- AincA® — Anesthesia Associates, Inc. · Class I
- AincA® — Anesthesia Associates, Inc. · Class I
- Portex — ICU MEDICAL, INC. · Class I
- Spiroguard with Integral Mouthpiece — GVS Filter Technology UK Ltd · Class IIa
- AincA® — Anesthesia Associates, Inc. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Instrumentation Industries, Incorporated
Sources (1)
- FDA UDI ea79b68a-1789-4c42-a8c9-32d97e20d720 35 fields · synced May 30, 2026