# GUANGZHOU WONDFO BIOTECH CO., LTD.

FEI: 3004635103
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: GUANGZHOU WONDFO BIOTECH CO., LTD. (#9064561)

Address: No.8 Lizhishan Road, Science City, Huangpu District, Guangzhou Guangdong, 510663, CN

Mandatory US Agent: LSI International Inc.

## Products

Total registered: 11
Top product codes: QBF, NGL, NFT, LCM, PTH, NGG, NFW, NFY, NFV, QAW, PTG
Regulation §: 862.3700, 862.3650, 862.3100, 862.3150, 862.3610, 862.3870, 862.3250, 862.3170, 862.3910, 862.3620

Proprietary names: PRIME SCREEN® Single Panel Urine Test Cannabinoids (THC20), SAFElife™ T-Dip Multi-Drug Urine Test Panel Dx

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004635103%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004635103