Taiwan FDA registration b3d4a26c28ea414eeef839e76443cf09

"ERKA" Manual Stethoscope (Non-sterile)

TW: "愛爾卡" 手動聽診器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ERKA. KALLMEYER MEDIZINTECHNIK GMBH & CO. KG·Registered Apr 14, 2017 – Apr 14, 2022Expired
Registration details
Analysis ID
b3d4a26c28ea414eeef839e76443cf09
License Form
Ministry of Health Medical Device Import No. 017708
Customs Code
DHA09401770806
Company information
Manufacturer Country
Germany
Authorized Representative
MEDICAL QI LTD.
Product details
Intended Use
Limited to the first-level identification range of the "stethoscope (E.1875)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E1875 stethoscope
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 14, 2017
Expiry Date
Apr 14, 2022
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About this record

Access comprehensive regulatory information for "ERKA" Manual Stethoscope (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b3d4a26c28ea414eeef839e76443cf09 and manufactured by ERKA. KALLMEYER MEDIZINTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is MEDICAL QI LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ERKA. KALLMEYER MEDIZINTECHNIK GMBH & CO. KG, 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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