Identity
- Trade Name
- Mojo TMT Holster Kit FDA UDI
- Generic Name
- Tourniquet cuff, single-use FDA UDI
- Device Name
- This kit treats Massive Hemorrhage and comes in nylon holster style belt pouch. The kit contains a tourniquet of choice. The pouch has a vertical belt loop and can be worn on your standard 2” wide utility and gun belts. FDA UDI
- Model / Reference
- 02 FDA UDI
- Description
- This kit treats Massive Hemorrhage and comes in nylon holster style belt pouch. The kit contains a tourniquet of choice. The pouch has a vertical belt loop and can be worn on your standard 2” wide utility and gun belts. FDA UDI
Identifiers
- Catalog Number
- 88-115-01 FDA UDI
- Primary DI / UDI-DI
- M6898811501020 FDA UDI
- FDA Product Code
- OHO FDA UDI
- GMDN Term
- Tourniquet cuff, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4014 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Tourniquet cuff, single-use
Mojo TMT Holster Kit by Safeguard Us Operating, Llc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Safeguard Us Operating, Llc
Sources (1)
- FDA UDI 97e01878-9516-4f3b-a433-04d8f5c61169 34 fields · synced Jun 6, 2026