Identity
- Trade Name
- Backorder Solutions FDA UDI
- Generic Name
- Arterial tourniquet, pneumatic FDA UDI
- Model / Reference
- 20-6110 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B504TQ2061100 FDA UDI
- FDA Product Code
- KCY FDA UDI
- GMDN Term
- Arterial tourniquet, pneumatic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.5910 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Arterial tourniquet, pneumatic
Backorder Solutions by Provision — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Arterial tourniquet, pneumatic.
- The Quick-T tourniquet — FIRST CARE PRODUCTS LTD · Class I
- GSO — Group Supply Organization Medical Technology(Shanghai) Ltd · Class I
- Quick-T — FIRST CARE PRODUCTS LTD · Class I
- GSO — Group Supply Organization Medical Technology(Shanghai) Ltd · Class I
- Zimmer — Provision · Class I
- Hammarplast Medical — Provision · Class I
- Backorder Solutions — Provision · Class I
- Zimmer — Provision · 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
- Provision
Sources (1)
- FDA UDI 614c5da4-6cf6-4b06-bded-f6f83a9f3016 33 fields · synced May 31, 2026