Taiwan FDA registration 028989cf732967cc72ca11905e143de1
Vivazer Osuction Dressings (Sterilized/Unsterilized)
TW: 維華澤吸滲敷料 (滅菌/未滅菌)
Taiwan·Risk Class 1·LOHMANN & RAUSCHER INTERNATIONAL GMBH & CO. KG·Registered Oct 20, 2017 – Oct 20, 2027ActiveRegistration details
- Analysis ID
- 028989cf732967cc72ca11905e143de1
- Customs Code
- DHA09401843400
Company information
- Manufacturer
- LOHMANN & RAUSCHER INTERNATIONAL GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- SEQPRO, INC.
Product details
- Intended Use
- Limited to the first level recognition range of the classification and grading management measures for medical equipment "hydrophilic trauma covering materials (I.4018)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4018 親水性創傷覆蓋材
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Oct 20, 2017
- Expiry Date
- Oct 20, 2027
About this record
Access comprehensive regulatory information for Vivazer Osuction Dressings (Sterilized/Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 028989cf732967cc72ca11905e143de1 and manufactured by LOHMANN & RAUSCHER INTERNATIONAL GMBH & CO. KG. The authorized representative in Taiwan is SEQPRO, INC..
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