Identity
- Trade Name
- SWAT-T Elastic Tourniquet, Black FDA UDI
- Generic Name
- Limb tourniquet, manual, single-use FDA UDI
- Device Name
- SWAT-T Elastic Tourniquet, used to stop or slow severe hemorrhaging from injured limbs and to reduce blood loss. FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- SWAT-T Elastic Tourniquet, used to stop or slow severe hemorrhaging from injured limbs and to reduce blood loss. FDA UDI
Identifiers
- Catalog Number
- SWAT-T-BLK-EA FDA UDI
- Primary DI / UDI-DI
- 00857048006392 FDA UDI
- FDA Product Code
- GAX FDA UDI
- GMDN Term
- Limb tourniquet, manual, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.5900 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
No
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: Limb tourniquet, manual, single-use
SWAT-T Elastic Tourniquet, Black by H & H Medical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Limb tourniquet, manual, single-use.
- Centurion — Centurion Medical Products · Class I
- SOF® TOURNIQUET GEN 4, COLOR-BLUE — TACTICAL MEDICAL SOLUTIONS, LLC · Class I
- Dealmed — DEALMED MEDICAL SUPPLIES LLC · Class I
- ZKSK — Beijing ZKSK Technology Co., Ltd · Class I
- Resilient Medical Solutions — Resilient Medical Solutions, LLC · Class I
- ASP MEDICAL — Asp Global, LLC · Class I
- Fisherbrand — FISHER SCIENTIFIC COMPANY L.L.C. · Class I
- Centurion — Centurion Medical Products · 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
- H & H Medical Corporation
Sources (1)
- FDA UDI 538d07f4-66bf-4ce7-94e2-11391f29c1b7 35 fields · synced May 30, 2026