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"Esres" half-moon cartilage suture repairer - Taiwan Registration 564498ddbb0b998f5b52e8b58dc0f90b

Access comprehensive regulatory information for "Esres" half-moon cartilage suture repairer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 564498ddbb0b998f5b52e8b58dc0f90b and manufactured by ARTHREX INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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564498ddbb0b998f5b52e8b58dc0f90b
Registration Details
Taiwan FDA Registration: 564498ddbb0b998f5b52e8b58dc0f90b
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Device Details

"Esres" half-moon cartilage suture repairer
TW: โ€œ่‰พๆ€็‘žๆ–ฏโ€ๅŠๆœˆ่ปŸ้ชจ็ธซๅˆไฟฎ่ฃœๅ™จ
Risk Class 2

Registration Details

564498ddbb0b998f5b52e8b58dc0f90b

DHA00602018701

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.5000 Non-absorbable polyethylene terephthalate sewing wire

import

Dates and Status

Sep 21, 2009

Sep 21, 2024