Taiwan FDA registration 2cf9cb611634a8ee00071d6420f5bd9a

"Cayenne" Orthopedic Manual Surgical Instrument (Sterile/Non-Sterile)

TW: "凱燕" 手動式骨科手術器械(滅菌/未滅菌)

Taiwan·Risk Class 1·MD·Cayenne Medical, Inc.·Registered Jun 15, 2018 – Jun 15, 2028Active

Registration details

Analysis ID: 2cf9cb611634a8ee00071d6420f5bd9a
License Form: Ministry of Health Medical Device Import No. 019195
Customs Code: DHA09401919500

Company information

Manufacturer: Cayenne Medical, Inc.
Manufacturer Country: United States
Authorized Representative: ZIMMER BIOMET TAIWAN CO., LTD.

Product details

Intended Use: Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N4540 Manual osteologic surgery instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 15, 2018
Expiry Date: Jun 15, 2028

About this record

Access comprehensive regulatory information for "Cayenne" Orthopedic Manual Surgical Instrument (Sterile/Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2cf9cb611634a8ee00071d6420f5bd9a and manufactured by Cayenne Medical, Inc.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..

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