← Back to catalogue
Mask Adult Non Rebreather Two Valves 7' Saflo Tubing
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Mask Adult Non Rebreather Two Valves 7' Saflo Tubing FDA UDI
- Generic Name
- Rebreathing oxygen face mask FDA UDI
- Device Name
- MASK ADULT NON REBREATHER TWO VALVES 7' SAFLO TUBING FDA UDI
- Model / Reference
- MS-2460S FDA UDI
- Description
- MASK ADULT NON REBREATHER TWO VALVES 7' SAFLO TUBING FDA UDI
Identifiers
- Catalog Number
- MS-2460S FDA UDI
- Primary DI / UDI-DI
- 00628725097770 FDA UDI
- FDA Product Code
- KGB FDA UDI
- GMDN Term
- Rebreathing oxygen face mask FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5570 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
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Rebreathing oxygen face mask
Mask Adult Non Rebreather Two Valves 7' Saflo Tubing by Canadian Hospital Specialties Limited — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Rebreathing oxygen face mask.
- DUAL MASK-ADULT MALE NOSE CLIP MC WITH CO2 MONIT 7FT (USA) — FLEXICARE MEDICAL LIMITED · Class II
- Curaplex — TRI-ANIM HEALTH SERVICES, INC. · Class I
- Ventlab — Ventlab Corp. · Class I
- Mask — Beijing Rongrui-Century Science & Technology Co. , Ltd. · Class IIa
- AMARA MASK WITH RS FRAME AND HEADGEAR LARGE, INTL — Respironics Inc. · Class IIa
- ClasStar, GanzGesMask, NIV, AAV, L — Drägerwerk AG & Co. KGaA · Class IIa
- Venticaire Lite — FLEXICARE MEDICAL LIMITED · Class I
- Oro-Nasal Mask — HANS RUDOLPH, INC. · Class IIa
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
- Canadian Hospital Specialties Limited
Sources (1)
- FDA UDI e27d81b7-c0c6-40d9-a2f8-ef2897151837 35 fields · synced May 30, 2026