Identity
- Trade Name
- T-RING Digit Tourniquet FDA UDI
- Generic Name
- Digit tourniquet, manual FDA UDI
- Device Name
- The T-RING is a non-pneumatic tourniquet for digits (fingers and toes). It is one size fits all, and automatically adjusts to the size of the digit to apply a safe and effective pressure (approximately 150 mm Hg) FDA UDI
- Model / Reference
- TR001 FDA UDI
- Description
- The T-RING is a non-pneumatic tourniquet for digits (fingers and toes). It is one size fits all, and automatically adjusts to the size of the digit to apply a safe and effective pressure (approximately 150 mm Hg) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10869193000016 FDA UDI
- FDA Product Code
- GAX FDA UDI
- GMDN Term
- Digit tourniquet, manual 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Radiation Sterilization FDA UDI
Category: Digit tourniquet, manual
T-RING Digit Tourniquet by Precision Medical Devices Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Digit tourniquet, manual.
- Tourni-Cot - Medium — Mar-Med Co. · Class I
- Tourni-Cot - Large — Mar-Med Co. · Class I
- Tourni-Cot - Small — Mar-Med Co. · Class I
- Tourni-Cot - Extra Large — Mar-Med Co. · Class I
- Tourni-Cot - Universal — Mar-Med Co. · Class I
- Susol® Ribbon Tourniquet — BAILEY INSTRUMENTS LTD · Class I
- T-RING FLEX Digit Tourniquet — Precision Medical Devices Inc · 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 |
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Manufacturer
- Manufacturer
- Precision Medical Devices Inc
Sources (1)
- FDA UDI c2076d18-6fc2-4e28-bda2-b8742dba1131 34 fields · synced May 30, 2026