# REPROLIFE INC.

FEI: 3013019894
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: REPROLIFE Inc. (#10054077)

Address: 2-5-3-9F Shinjuku, Shinjuku-ku Tokyo, 160-0022, JP

Mandatory US Agent: Globizz Corp

## Products

Total registered: 1
Top product codes: MQK
Regulation §: 884.6160

Proprietary names: Cryotec (4 pieces) (Blue), Cryotec (10 pieces) (White), Cryotec (10 pieces) (Yellow), Cryotec (10 pieces) (Red), Cryotec (4 pieces) (Red), Cryotec (4 pieces) (White), Cryotec (10 pieces) (Blue), Cryotec (10 pieces) (Green), Cryotec (4 pieces) (Yellow), Cryotec (4 pieces) (Green)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223013019894%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3013019894