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Intravenous-Intraosseous Kit (TMK-IV/IO), Refill, Contents Only
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Intravenous-Intraosseous Kit (TMK-IV/IO), Refill, Contents Only FDA UDI
- Generic Name
- Peripheral intravenous catheterization support kit FDA UDI
- Device Name
- The TMK-IV/IO is designed to conveniently house essential intravenous (IV) and intraosseous (IO) infusion supplies and medications for tactical missions. FDA UDI
- Model / Reference
- 01323REF FDA UDI
- Description
- The TMK-IV/IO is designed to conveniently house essential intravenous (IV) and intraosseous (IO) infusion supplies and medications for tactical missions. FDA UDI
Identifiers
- Catalog Number
- 01323REF FDA UDI
- Primary DI / UDI-DI
- 00850018892773 FDA UDI
- FDA Product Code
- LRS FDA UDI
- GMDN Term
- Peripheral intravenous catheterization support kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5200 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
Yes
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Category: Peripheral intravenous catheterization support kit
Intravenous-Intraosseous Kit (TMK-IV/IO), Refill, Contents Only by Altitude Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID
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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
- Altitude Technologies Inc.
Sources (1)
- FDA UDI 7fa203fb-f131-40c2-8d29-cfe2ac7e2409 35 fields · synced May 30, 2026