Taiwan FDA registration f1f45ab09404df30005ac2859f60fb13
"Axon" decompression mattress
TW: "艾克森" 減壓床墊
Taiwan·Risk Class 1·ACTION PRODUCTS, INC.·Registered Jun 13, 2005 – Jun 13, 2010CancelledRegistration details
- Analysis ID
- f1f45ab09404df30005ac2859f60fb13
- Customs Code
- DHA04400017107
Company information
- Manufacturer
- ACTION PRODUCTS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
Product details
- Intended Use
- Treat or avoid bedridden bed.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- import
Dates and status
- Registration Date
- Jun 13, 2005
- Expiry Date
- Jun 13, 2010
- 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 "Axon" decompression mattress in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f1f45ab09404df30005ac2859f60fb13 and manufactured by ACTION PRODUCTS, INC.. 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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