Identity
- Trade Name
- Gongdong FDA UDI
- Generic Name
- General laboratory container, single-use FDA UDI
- Device Name
- TEST TUBE, 12x75, PP FDA UDI
- Model / Reference
- G10301 FDA UDI
- Description
- TEST TUBE, 12x75, PP FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06947462400259 FDA UDI
- FDA Product Code
- LXG FDA UDI
- GMDN Term
- General laboratory container, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2050 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
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: General laboratory container, single-use
Gongdong by Zhejiang Gongdong Medical Technology Co., Ltd., — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Zhejiang Gongdong Medical Technology Co., Ltd.,
Sources (1)
- FDA UDI e30b2c5f-9952-4531-a89f-3dcc2c65629a 33 fields · synced May 30, 2026