Taiwan FDA registration cef1ca749ab1d3295248dd0dbc7fef22

"Thunderbolt" is a general suction tube

TW: "霹霖" 一般抽吸管

Taiwan·Risk Class 1·PILLING SURGICAL·Registered Dec 29, 2005 – Dec 29, 2010Cancelled

Registration details

Analysis ID: cef1ca749ab1d3295248dd0dbc7fef22
Customs Code: DHA04400243502

Company information

Manufacturer: PILLING SURGICAL
Manufacturer Country: United States
Authorized Representative: SUNSHINE INSTRUMENT LTD.

Product details

Intended Use: ENT manual surgical instruments are various equipment used to examine and treat the bronchi, esophagus, trachea, larynx, pharynx, nasal paranasal sinuses and ears during surgery.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4420 Otolaryngology manual surgical instruments
Import Information: import

Dates and status

Registration Date: Dec 29, 2005
Expiry Date: Dec 29, 2010
Cancellation Date: Nov 30, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Thunderbolt" is a general suction tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cef1ca749ab1d3295248dd0dbc7fef22 and manufactured by PILLING SURGICAL. The authorized representative in Taiwan is SUNSHINE INSTRUMENT LTD..

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