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"Bidi" lumbar puncture needle - Taiwan Registration 336dd5f08f6010e57b133cc1dc31e207

Access comprehensive regulatory information for "Bidi" lumbar puncture needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 336dd5f08f6010e57b133cc1dc31e207 and manufactured by BECTON DICKINSON AND COMPANY;; BD CARIBE LTD.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BECTON DICKINSON, S.A., and 1 recent registrations in the same category. 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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336dd5f08f6010e57b133cc1dc31e207
Registration Details
Taiwan FDA Registration: 336dd5f08f6010e57b133cc1dc31e207
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Device Details

"Bidi" lumbar puncture needle
TW: "ๅฟ…ๅธ" ่…ฐๆคŽ็ฉฟๅˆบ้‡
Risk Class 2

Registration Details

336dd5f08f6010e57b133cc1dc31e207

DHA00601114905

Company Information

Product Details

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

D Anesthesiology

import

Dates and Status

Apr 04, 2005

Apr 04, 2030

Companies Making Similar Products
Top companies providing products similar to ""Bidi" lumbar puncture needle"

BECTON DICKINSON, S.A.

1 products

Latest registration: Sep 12, 2002

Recent Registrations
Recently registered similar products

"Bidi" lumbar puncture needle

Sep 12, 2002
Manufacturer:

BECTON DICKINSON, S.A.

Registration:

732d99a9a0e19629b25f40a5bc4dd481

Risk Class:

2