Identity
- Trade Name
- Tubing, Smooth Interior, Disposable, 22MM-60" FDA UDI
- Generic Name
- High-pressure medical gas hose FDA UDI
- Device Name
- Tubing, Smooth Interior, Disposable, 22MM-60" FDA UDI
- Model / Reference
- Tubing, Smooth Interior, Disposable, 22MM-60" - 243703 FDA UDI
- Description
- Tubing, Smooth Interior, Disposable, 22MM-60" FDA UDI
Identifiers
- Catalog Number
- 243703 FDA UDI
- Primary DI / UDI-DI
- 00817081024722 FDA UDI
- FDA Product Code
- BYX FDA UDI
- GMDN Term
- High-pressure medical gas hose FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5860 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: High-pressure medical gas hose
Tubing, Smooth Interior, Disposable, 22MM-60" by A-M Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as High-pressure medical gas hose.
- Terumo® Advanced Perfusion System 1 — Terumo Cardiovascular Systems Corporation · Class I
- CO2 Hose and Yoke Shuttle Valve System — Northgate Technologies Inc. · Class II
- Quality Connect HD — DEHAS Medical Systems GmbH · Class I
- Oxygen Accessory — SUNSET HEALTHCARE SOLUTIONS, Inc. · Class I
- Terumo® Advanced Perfusion System 1 — Terumo Cardiovascular Systems Corporation · Class I
- Controller, Full/Swipe — C2 Therapeutics, Inc. · Class II
- Terumo® Advanced Perfusion System 1 — Terumo Cardiovascular Systems Corporation · Class I
- Quality Connect HD — DEHAS Medical Systems GmbH · 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
- A-M Systems, Inc.
Sources (1)
- FDA UDI acea1dec-1f7a-4ef9-8f9a-8f4d30119742 35 fields · synced May 30, 2026