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DiaClon Anti-M - Taiwan Registration 21bdc38f88a2c62b4745e6e01e124b1a

Access comprehensive regulatory information for DiaClon Anti-M in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21bdc38f88a2c62b4745e6e01e124b1a and manufactured by DIAMED GMBH. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).

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21bdc38f88a2c62b4745e6e01e124b1a
Registration Details
Taiwan FDA Registration: 21bdc38f88a2c62b4745e6e01e124b1a
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Device Details

DiaClon Anti-M
TW: "ไผฏ็‘ž" ๅ–ฎๆ ชๆŠ—้ซ”ๆŠ—M้‘‘ๅฎšๅก็‰‡
Risk Class 2
MD

Registration Details

21bdc38f88a2c62b4745e6e01e124b1a

Ministry of Health Medical Device Import No. 035680

DHA05603568005

Company Information

Switzerland

Product Details

Antigen-antibody response is used to detect M antigen on red blood cells.

B Hematology, pathology, and genetics

B4020 Analyze specific reagents

Imported from abroad; GMP

Dates and Status

Jul 20, 2022

Jul 20, 2027