Philippines FDA registration MDR-04916F

Anspatch™ G1 Dissection Tools, Fluted Router

Name: Anspatch™ G1 Dissection Tools, Fluted Router — Philippines FDA registration MDR-04916F
Creator: The Anspach Effort, Inc. 4500 Riverside Drive, Palm Beach Gardens, Florida, 33410, USA
Keywords: Anspatch™ G1 Dissection Tools, Fluted Router, MDR-04916F, The Anspach Effort, Inc. 4500 Riverside Drive, Palm Beach Gardens, Florida, 33410, USA, Johnson & Johnson (Phils.) Inc., USA, Philippines FDA registration

PhilippinesThe Anspach Effort, Inc. 4500 Riverside Drive, Palm Beach Gardens, Florida, 33410, USAUSAIssued October 10, 2022 – November 16, 2027

VerifiedFDA Philippines · official registry

Device information

Product Name: Anspatch™ G1 Dissection Tools, Fluted Router
Registration Number: MDR-04916F

Manufacturer details

Manufacturer: The Anspach Effort, Inc. 4500 Riverside Drive, Palm Beach Gardens, Florida, 33410, USA
Country of Origin: USA

Importer & distribution

Importer/Distributor: Johnson & Johnson (Phils.) Inc.

Registration dates

Issuance Date: October 10, 2022
Expiry Date: November 16, 2027

About this record

Access comprehensive regulatory information for Anspatch™ G1 Dissection Tools, Fluted Router in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04916F and manufactured by The Anspach Effort, Inc. 4500 Riverside Drive, Palm Beach Gardens, Florida, 33410, USA in USA. The device was registered on October 10, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Johnson & Johnson (Phils.) Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.