Pure Global

"Midmark" Central Vacuum (Non-Sterile) - Taiwan Registration fa335838d8a122dc7e2c898a01af261d

Access comprehensive regulatory information for "Midmark" Central Vacuum (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 fa335838d8a122dc7e2c898a01af261d and manufactured by MIDMARK CORPORATION. The authorized representative in Taiwan is KOLN BIO-MEDICAL 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
fa335838d8a122dc7e2c898a01af261d
Registration Details
Taiwan FDA Registration: fa335838d8a122dc7e2c898a01af261d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Midmark" Central Vacuum (Non-Sterile)
TW: "ๅ้ฆฌๅ…‹" ไธญๅคฎ่ฒ ๅฃ“ๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

fa335838d8a122dc7e2c898a01af261d

Ministry of Health Medical Device Import No. 019168

DHA09401916800

Company Information

United States

Product Details

Limited to the first level identification range of dental surgical devices and their accessories (F.6640) under the Measures for the Administration of Medical Devices.

F Dental devices

F6640 Dental Surgical Devices and Their Accessories

Imported from abroad

Dates and Status

Jun 12, 2018

Jun 12, 2023