Taiwan FDA registration 064da3f894fc1734b9b42c66e556767c

"Braun" lumbar spine anesthesia with a puncture needle

TW: “柏朗”腰椎麻醉用穿刺針
Taiwan flagTaiwan·Risk Class 2·B.BRAUN MELSUNGEN AG;; B. Braun Aesculap Japan Co., Ltd. Tochigi Factory·Registered Jul 03, 2012 – Jul 03, 2017Cancelled
Registration details
Analysis ID
064da3f894fc1734b9b42c66e556767c
Customs Code
DHA00602375402
Company information
Manufacturer Country
Germany;;Japan
Authorized Representative
B. BRAUN TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5150 麻醉傳輸穿刺針
Import Information
import
Dates and status
Registration Date
Jul 03, 2012
Expiry Date
Jul 03, 2017
Cancellation Date
Nov 20, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Braun" lumbar spine anesthesia with a 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 064da3f894fc1734b9b42c66e556767c and manufactured by B.BRAUN MELSUNGEN AG;; B. Braun Aesculap Japan Co., Ltd. Tochigi Factory. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including B. BRAUN MEDICAL INDUSTRIES SDN. BHD.;; B. BRAUN MELSUNGEN AG, B. BRAUN MELSUNGEN AG., and 2 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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