Identity
- Trade Name
- ProCure FDA UDI
- Generic Name
- Non-rebreathing oxygen face mask FDA UDI
- Device Name
- ProCure Non-Rebreather Mask High Concentration w/7' Tubing 750ml ReserviorvBag Standard Connector Pediatric FDA UDI
- Model / Reference
- 1006440 FDA UDI
- Description
- ProCure Non-Rebreather Mask High Concentration w/7' Tubing 750ml ReserviorvBag Standard Connector Pediatric FDA UDI
Identifiers
- Catalog Number
- 1006440 FDA UDI
- Primary DI / UDI-DI
- 10840330704455 FDA UDI
- FDA Product Code
- KGB FDA UDI
- GMDN Term
- Non-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
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
Dimensions & Sizes
- Size
- Length — 7 Feet FDA UDI
Category: Non-rebreathing oxygen face mask
ProCure by Twin Med, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Non-rebreathing oxygen face mask.
- POM EZ-Lite — Stryker Corp. · Class II
- BF — Allied Medical LLC · Class I
- Rescuer O-Mask — B.L.S. Systems Limited · Class I
- Resp-O2 Oxygen Mask High-Concentration, Elongated Adult — Dynarex Corp. · Class I
- BF — Allied Medical LLC · Class I
- Procedural Oxygen Mask — Stryker Corp. · Class II
- Curaplex — BOUND TREE MEDICAL, LLC · Class I
- Ventlab — Ventlab Corp. · 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
- Twin Med, LLC
Sources (1)
- FDA UDI 5cacdbeb-f336-4640-b145-931f3498fa32 36 fields · synced Jun 8, 2026