Identity
- Trade Name
- GENTEC® FDA UDI
- Generic Name
- Surgical suction system collection container, reusable FDA UDI
- Device Name
- SJ-1500 is the suction jar which is used to collect pus, blood clots, phlegm, and excess fluids by connecting to a patient on one end, and vacuum source (such as suction regulator) on the other FDA UDI
- Model / Reference
- SJ-1500 FDA UDI
- Description
- SJ-1500 is the suction jar which is used to collect pus, blood clots, phlegm, and excess fluids by connecting to a patient on one end, and vacuum source (such as suction regulator) on the other FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06970966663110 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Surgical suction system collection container, reusable 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
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical suction system collection container, reusable
Gentec® by Gentec(shanghai)corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Gentec(shanghai)corporation
Sources (1)
- FDA UDI a16261b8-a842-4e12-90fc-18792a96ad97 34 fields · synced May 30, 2026