Identity
- Trade Name
- BLEED CONTROL KIT FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Device Name
- Windless Tourniquet Elastic Band Back-Up Tourniquet Hema-Seal Trauma Dressing Emergency Blanket Trauma Pad Nitrile Exam Gloves Bandage Shears to Cut Clothing Marker to Note Tourniquet Time Bleeding Control Product Use Guidelines Wall Mounting Kit FDA UDI
- Model / Reference
- S-25331 FDA UDI
- Description
- Windless Tourniquet Elastic Band Back-Up Tourniquet Hema-Seal Trauma Dressing Emergency Blanket Trauma Pad Nitrile Exam Gloves Bandage Shears to Cut Clothing Marker to Note Tourniquet Time Bleeding Control Product Use Guidelines Wall Mounting Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10850015055482 FDA UDI
- FDA Product Code
- OHO FDA UDI
- GMDN Term
- First aid kit, non-medicated, 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
No
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: First aid kit, non-medicated, single-use
Bleed Control Kit by Uline, Inc. — 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
- Uline, Inc.
Sources (1)
- FDA UDI 6444933f-6b9b-407a-b768-d7b5c2d97a0b 33 fields · synced Jun 8, 2026