← Back to catalogue
22mm Compact Breathing System With Luer Elbow. 2.0m
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- 22MM COMPACT BREATHING SYSTEM WITH LUER ELBOW. 2.0M FDA UDI
- Generic Name
- Anaesthesia breathing circuit, reusable FDA UDI
- Device Name
- 22MM COMPACT BREATHING SYSTEM WITH LUER ELBOW. 2.0M FDA UDI
- Model / Reference
- 2151800 FDA UDI
- Description
- 22MM COMPACT BREATHING SYSTEM WITH LUER ELBOW. 2.0M FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05030267063338 FDA UDI
- FDA Product Code
- CAI FDA UDI
- GMDN Term
- Anaesthesia breathing circuit, reusable 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
No
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, reusable
22mm Compact Breathing System With Luer Elbow. 2.0m by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Anaesthesia breathing circuit, reusable.
- Ultipor™ Anesthesia Breathing Circuit System - Adult Machine Kit — Global Life Sciences Solutions USA LLC · Class II
- MATRX SCAV, W/SM HOOD(WO/SHUTOF — Parker Hannifin Corp. · Class I
- AirTechniques — Baldus Sedation GmbH & Co. KG · Class I
- Sil.Plus — Galemed Corp. · Class I
- PORTER/BRN ADULT RG ASSY ONLY — Parker Hannifin Corp. · Class I
- Ultipor™ Anesthesia Breathing Circuit System - Adult Machine Kit — Global Life Sciences Solutions USA LLC · Class II
- Ultipor™ Anesthesia Breathing Circuit System - Pediatric Machine Kit — Global Life Sciences Solutions USA LLC · Class II
- Trulink — SPACELABS HEALTHCARE (WASHINGTON), INC · Class II
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 ab6d58d9-bceb-4f2f-a07c-4cbf741e6208 34 fields · synced May 30, 2026