← Back to catalogue
15mm Flextube Breathing System With Luer Elbow. 1.6m
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- 15MM FLEXTUBE BREATHING SYSTEM WITH LUER ELBOW. 1.6M FDA UDI
- Generic Name
- Anaesthesia breathing circuit, single-use FDA UDI
- Device Name
- 15MM FLEXTUBE BREATHING SYSTEM WITH LUER ELBOW. 1.6M FDA UDI
- Model / Reference
- 2142000 FDA UDI
- Description
- 15MM FLEXTUBE BREATHING SYSTEM WITH LUER ELBOW. 1.6M FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05030267062935 FDA UDI
- FDA Product Code
- CAI FDA UDI
- GMDN Term
- Anaesthesia breathing circuit, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5240 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Anaesthesia breathing circuit, single-use
15mm Flextube Breathing System With Luer Elbow. 1.6m by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Anaesthesia breathing circuit, single-use.
- Vital Signs™ — Airlife, Inc. · Class II
- HUDSON RCI — TELEFLEX INCORPORATED · Class I
- Vital Signs™ — Airlife, Inc. · Class I
- UNIVERSAL FLEX2®BREATHING CIRCUIT & PACK KIT — KING SYSTEMS CORPORATION. · Class I
- Vital Signs™ — Airlife, Inc. · Class I
- Portex — ICU MEDICAL, INC. · Class I
- UNIVERSAL FLEX2® — KING SYSTEMS CORPORATION. · Class I
- PEDIATRIC ULTRA FLEX® — KING SYSTEMS CORPORATION. · 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
- Intersurgical Incorporated
Sources (1)
- FDA UDI 419260be-3420-4183-8502-c8ce28a99ab5 34 fields · synced May 31, 2026