Taiwan FDA registration 8d3c211d7d7327329b0129964bb5f64d
"Bruder" cold compress pack (unsterilized)
TW: “布魯德”冷敷包 (未滅菌)
Registration details
- Analysis ID
- 8d3c211d7d7327329b0129964bb5f64d
- Customs Code
- DHA04400538400
Company information
- Manufacturer
- BRUDER HEALTHCARE COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5700 醫療用冷熱敷裝置
- Import Information
- import
Dates and status
- Registration Date
- Nov 28, 2006
- Expiry Date
- Nov 28, 2011
- Cancellation Date
- Nov 08, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bruder" cold compress pack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8d3c211d7d7327329b0129964bb5f64d and manufactured by BRUDER HEALTHCARE COMPANY. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.
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.
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