Taiwan FDA registration 7cbf1bbf5df3e54589695c8ce1e8360c

"Marco Code" Heat Sealing Equipment (Unsterilized)

TW: "馬可法碼" 加熱密封器材 (未滅菌)

Taiwan·Risk Class 1·MACOPHARMA·Registered Oct 28, 2011 – Oct 28, 2016Cancelled

Registration details

Analysis ID: 7cbf1bbf5df3e54589695c8ce1e8360c
Customs Code: DHA04401099000

Company information

Manufacturer: MACOPHARMA
Manufacturer Country: France
Authorized Representative: Y.H. BIOTEK CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Heating and Sealing Equipment (B.9750)".
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9750 Heat-sealing equipment
Import Information: import

Dates and status

Registration Date: Oct 28, 2011
Expiry Date: Oct 28, 2016
Cancellation Date: Jun 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Marco Code" Heat Sealing Equipment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7cbf1bbf5df3e54589695c8ce1e8360c and manufactured by MACOPHARMA. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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.