Taiwan FDA registration eb44e7c0d7b170e8e84d20fb2b424d61

Schbier Blood Pen

TW: 施比爾採血筆
Taiwan flagTaiwan·Risk Class 1·SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.·Registered Mar 01, 2006 – Mar 01, 2011Cancelled
Registration details
Analysis ID
eb44e7c0d7b170e8e84d20fb2b424d61
Customs Code
DHA04600011806
Company information
Manufacturer Country
China
Authorized Representative
BIONIME CORPORATION
Product details
Intended Use
The fixed lancet also assists the lancet to puncture the skin and collect a small amount of blood samples.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Hand Instruments for General Surgery
Import Information
Chinese goods;; input
Dates and status
Registration Date
Mar 01, 2006
Expiry Date
Mar 01, 2011
Cancellation Date
Oct 29, 2012
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 Schbier Blood Pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eb44e7c0d7b170e8e84d20fb2b424d61 and manufactured by SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is BIONIME CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD., 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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