Identity
- Trade Name
- Sinton Medical Products FDA UDI
- Generic Name
- Radiographic procedure tubing FDA UDI
- Device Name
- 21" transfer set for Contrast with ball check valve spike and C-Clamp with female luer connector FDA UDI
- Model / Reference
- 700207-2B FDA UDI
- Description
- 21" transfer set for Contrast with ball check valve spike and C-Clamp with female luer connector FDA UDI
Identifiers
- Catalog Number
- HT-SK500FC FDA UDI
- Primary DI / UDI-DI
- 06938327909826 FDA UDI
- FDA Product Code
- DXT FDA UDI
- GMDN Term
- Radiographic procedure tubing FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1650 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Radiographic procedure tubing
Sinton Medical Products by Shenzhen Boon Medical Supply Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Radiographic procedure tubing.
- Merit Medical® — Merit Medical Systems, Inc. · Class II
- High Pressure Tubing, Keep™ — Merit Medical Systems, Inc. · Class II
- Coeur Acist — Coeur, Inc. · Class II
- MEDRAD® Avanta Single Patient Disposable Set - Transducer Compatable — Bayer Medical Care Inc. · Class II
- MRI Integral "T" with Check Valve for MEDRAD® Spectris MR Injector — Bayer Medical Care Inc. · Class II
- Antmed — ShenZhen Antmed Co., Ltd · Class II
- Merit Medical® — Merit Medical Systems, Inc. · Class II
- Merit Medical® — Merit Medical Systems, Inc. · Class II
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Shenzhen Boon Medical Supply Co., Ltd.
Sources (1)
- FDA UDI 0d63a5cc-c0cf-4c7a-a60d-913bc01bc029 36 fields · synced May 30, 2026