Taiwan FDA registration bfc9d05130e932996930fde25a0e0d2a

Cardiopulmonary awakener

TW: 心肺蘇醒器
Taiwan flagTaiwan·MICHIGAN INSTRUMENTS INC·Registered Oct 04, 1982 – Oct 04, 1987Cancelled
Registration details
Analysis ID
bfc9d05130e932996930fde25a0e0d2a
Customs Code
DHA00600225809
Company information
Manufacturer Country
United States
Authorized Representative
TUNG FENG CO., LTD.
Product details
Product Type (Level 1)
0210 Cardiopulmonary awakener
Import Information
import
Dates and status
Registration Date
Oct 04, 1982
Expiry Date
Oct 04, 1987
Cancellation Date
Feb 26, 1990
Cancellation information
Status
Logged out
Reason
有效期限已屆
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About this record

Access comprehensive regulatory information for Cardiopulmonary awakener in Taiwan's medical device market through Pure Global AI's free database. is registered under number bfc9d05130e932996930fde25a0e0d2a and manufactured by MICHIGAN INSTRUMENTS INC. The authorized representative in Taiwan is TUNG FENG CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including SIEMENS AKTIENGESELLSCHAFT, BRUNSWICK BIOMEDICAL TECHNOLOGIES, INC., and 4 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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