Identity
- Trade Name
- Color Cuff FDA UDI
- Generic Name
- Tourniquet cuff, reusable FDA UDI
- Device Name
- Non-Sterile Reusable Tourniquet Cuff Dual Bladder, Dual Port and Quick Connect Connector FDA UDI
- Model / Reference
- 5922024245 FDA UDI
- Description
- Non-Sterile Reusable Tourniquet Cuff Dual Bladder, Dual Port and Quick Connect Connector FDA UDI
Identifiers
- Catalog Number
- 5922-024-245 FDA UDI
- Primary DI / UDI-DI
- 07613154600038 FDA UDI
- FDA Product Code
- KCY FDA UDI
- GMDN Term
- Tourniquet cuff, reusable 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
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 24.0 Inch FDA UDIWidth — 5.5 Inch FDA UDI
Category: Tourniquet cuff, reusable
Color Cuff by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tourniquet cuff, reusable.
- Vari-Fit Reusable — Delfi Medical Innovations Inc · Class I
- Reusable Conical Cuff — Zhejiang Longyou Lande Medical Technology Co., Ltd. · Class I
- Easi-Fit BFR, Reusable — Delfi Medical Innovations Inc · Class I
- Reusable Tourniquet Cuff — Zhejiang Longyou Lande Medical Technology Co., Ltd. · Class I
- Reusable Tourniquet Cuff — Zhejiang Longyou Lande Medical Technology Co., Ltd. · Class I
- ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP. · Class I
- Vari-Fit Reusable — Delfi Medical Innovations Inc · Class I
- Easi-Fit Reusable — Delfi Medical Innovations 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 154c2624-7eec-4cc8-9d06-213ad90c15d9 36 fields · synced Jun 6, 2026