Identity
- Trade Name
- ProCure FDA UDI
- Generic Name
- Oxygen administration tubing FDA UDI
- Device Name
- ProCure Oxygen Tubing Crush Resistant Standard Connector 21' KROT FDA UDI
- Model / Reference
- 1006461 FDA UDI
- Description
- ProCure Oxygen Tubing Crush Resistant Standard Connector 21' KROT FDA UDI
Identifiers
- Catalog Number
- 1006461 FDA UDI
- Primary DI / UDI-DI
- 10840330704660 FDA UDI
- FDA Product Code
- GAZ FDA UDI
- GMDN Term
- Oxygen administration tubing FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 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 — 21 Feet FDA UDI
Category: Oxygen administration tubing
ProCure by Twin Med, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Twin Med, LLC
Sources (1)
- FDA UDI d8209fe7-4c3e-4484-ab10-09e4e0c8c07e 36 fields · synced Jun 1, 2026