Taiwan FDA registration dd8f0285b984a51d2c6e6262118b75c4

"Zeiss" colposcopy

TW: “蔡司”陰道鏡
Taiwan flagTaiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered Jan 13, 2016 – Jan 13, 2021Cancelled
Registration details
Analysis ID
dd8f0285b984a51d2c6e6262118b75c4
Customs Code
DHA05602814100
Company information
Manufacturer Country
Germany
Authorized Representative
TAIWAN INSTRUMENT CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
l Obstetrics and Gynecology
Product Type (Level 2)
L.1630 Yin Mirror
Import Information
import
Dates and status
Registration Date
Jan 13, 2016
Expiry Date
Jan 13, 2021
Cancellation Date
Sep 23, 2023
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Zeiss" colposcopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd8f0285b984a51d2c6e6262118b75c4 and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARL ZEISS SURGICAL GMBH, 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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