FDA Registration
Active
🇨🇳 China
iScreen" Multi-Drug Urine Test Cup
Reg #: 3004635103
·
FEI: 3004635103
·
Expires 2025
Products
1
Proprietary Names
8
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- GUANGZHOU WONDFO BIOTECH CO., LTD.
- Registration Number
- 3004635103
- FEI Number
- 3004635103
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- No.8 Lizhishan Road, Science City, Huangpu District
- City
- Guangzhou Guangdong
- Country
- CN
Owner / Operator
- Firm Name
- GUANGZHOU WONDFO BIOTECH CO., LTD.
- Operator Number
- 9064561
- Address
- No.8 lizhishan Road, Science City, Huangpu District, 510663
- City
- GUANGZHOU
- State
- Guangdong
- Postal Code
- 510663
- Country
- CN
- Correspondent
- Jihua - Wang
US Agent
- Business Name
- LSI International Inc.
- Contact Name
- Joe Shia
- Address
- 504 East Diamond Ave., Suite I
- City
- Gaithersburg
- State
- MD
- ZIP
- 20877
- Country
- US
- [email protected]
- Phone
- 240 5057880
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Test, Methadone, Employment And Insurance Testing, Exempt | PVE | Class 2 | Clinical Toxicology | No | 2018-01-18 |
Proprietary Names
iScreen" Multi-Drug Urine Test Cup
STATSWAB® III Oral Fluid Drug Test
UScreen
iSCREEN ORAL FLUID TEST DRUG SCREEN CUBE
SAFElife T-Square Multi-Drug Oral Fluid Test
Prime Screen One Step Multi-Drug Oral Fluid Test
T-Cube Oral Fluid Drug Test
PRIME SCREEN® One Step Multi-Drug Oral Fluid Test
Establishment Types
Manufacture Medical Device