Taiwan FDA registration 37edd253dbd20698f8df1be84939de97

Johnson & Johnson in vitro prosthetic components (unsterilized)

TW: “強生”體外肢體義肢用組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·PEL SUPPLY CO.·Registered Mar 24, 2010 – Mar 24, 2025Cancelled
Registration details
Analysis ID
37edd253dbd20698f8df1be84939de97
Customs Code
DHA04400864300
Company information
Manufacturer
PEL SUPPLY CO.
Manufacturer Country
United States
Authorized Representative
JOHNSON A. L. TRADING CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of components for in vitro limb prosthetics (O.3420) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3420 體外肢體義肢用組件
Import Information
import
Dates and status
Registration Date
Mar 24, 2010
Expiry Date
Mar 24, 2025
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for Johnson & Johnson in vitro prosthetic components (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 37edd253dbd20698f8df1be84939de97 and manufactured by PEL SUPPLY CO.. The authorized representative in Taiwan is JOHNSON A. L. TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including FRIDDLE "S ORTHOPEDIC APPLIANCES, BLATCHFORD PRODUCTS LTD., and 5 recent registrations in the same category. 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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