Identity
- Trade Name
- TQ™ RAM FDA UDI
- Generic Name
- Pressure bandage, non-latex, single-use FDA UDI
- Device Name
- The device is intended for use in controlling compressible hemorrhage in areas not amendable to limb tourniquets and providing hands-free compression on top of a packed wound when attached to the TMT Tourniquet. FDA UDI
- Model / Reference
- 3 FDA UDI
- Description
- The device is intended for use in controlling compressible hemorrhage in areas not amendable to limb tourniquets and providing hands-free compression on top of a packed wound when attached to the TMT Tourniquet. FDA UDI
Identifiers
- Catalog Number
- 31-150 FDA UDI
- Primary DI / UDI-DI
- M68931150030 FDA UDI
- FDA Product Code
- MHW FDA UDI
- GMDN Term
- Pressure bandage, non-latex, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5075 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: Pressure bandage, non-latex, single-use
Tq™ Ram 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 34b7cab2-345c-4555-8802-8a6ad04b4c59 34 fields · synced Jun 8, 2026