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"Dengli" diagnostic X-ray tube sleeve assembly - Taiwan Registration 76cc97264275005ae790cdb5beb2be82

Access comprehensive regulatory information for "Dengli" diagnostic X-ray tube sleeve assembly in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 76cc97264275005ae790cdb5beb2be82 and manufactured by DUNLEE. The authorized representative in Taiwan is PAN ASIA INTERNATIONAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DUNLEE MEDICAL COMPONENTS, and 1 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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76cc97264275005ae790cdb5beb2be82
Registration Details
Taiwan FDA Registration: 76cc97264275005ae790cdb5beb2be82
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Device Details

"Dengli" diagnostic X-ray tube sleeve assembly
TW: "็™ป้‡Œ"่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ
Risk Class 1
Cancelled

Registration Details

76cc97264275005ae790cdb5beb2be82

DHAS4400279906

Company Information

United States

Product Details

The Diagnostic X-ray Tube Sleeve Assembly is an X-ray generating tube enclosed in a radiation protection device for diagnostic purposes.

P Radiology Science

P.1760 ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Mar 07, 2006

Mar 07, 2011

Jul 10, 2006

Cancellation Information

Logged out

่‡ช่ซ‹่จป้Šท

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