Identity
- Trade Name
- XinjingProWellness™ FDA UDI
- Generic Name
- General-purpose surgical suction system, vacuum FDA UDI
- Model / Reference
- 1010-C FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06973881680026 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- General-purpose surgical suction system, vacuum FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 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
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
No
FDA UDI
Category: General-purpose surgical suction system, vacuum
XinjingProWellness™ by Tianjin Newtrans Technology Development — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General-purpose surgical suction system, vacuum.
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- AURORA Evacuator — REBOUND THERAPEUTICS, CORPORATION · Class II
- GOMCO — Allied Medical LLC · Class II
- Orthopaedic Suction Set — GCMEDICA ENTERPRISE LTD.(WUXI) · Class II
- Schuco — Allied Medical LLC · Class II
- ADULT TIP SUCKER HEX HANDLE WITH VENT — NOVOSCI CORP. · Class II
- TIP SUCKER — NOVOSCI CORP. · 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 |
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Manufacturer
- Manufacturer
- Tianjin Newtrans Technology Development
Sources (1)
- FDA UDI c8e26b0a-af9d-4034-b1b2-7a0b1ad30516 32 fields · synced Jun 8, 2026