Taiwan FDA registration ceb2dfe25b2cdf94fa2baa97297e1e31
"Cardino" manual instruments for general surgery (unsterilized)
TW: "卡迪諾"一般手術用手動式器械(未滅菌)
Registration details
- Analysis ID
- ceb2dfe25b2cdf94fa2baa97297e1e31
- Customs Code
- DHA04400281802
Company information
- Manufacturer
- CARDINAL HEALTH 200, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Mitutoyo Medical Equipment Co., Ltd
Product details
- Intended Use
- Manual instruments for general surgery are non-powered, hand-held or hand-operated instruments that can be reused or thrown away after use, and are used for various general surgeries. Instruments include applicators, clips, living tissue brushes, hand-held dermabrasion brushes, scrapers, cannulas, suture holders, chisels, clips, shorteners, scrapers, cutters, separators, screwdrivers, skin graft dilators, frustration knives, tweezers, gouges, instrument guides, needle guides, hammers, hemostats, amputation hooks, suture needle knotting equipment, knives, blood lancets, mallets, Disposable or reusable suction and injection needles and sutures, bone knives, clips, files, maintainers, retractors, saws, scalpel blades, scalpel handles, one-piece scalpels, ring blades, mixing knives, U-nails, disposable or reusable strippers, through-tube needles, suture instruments for gastrointestinal use, measuring tapes and calipers. Surgical instruments used in other specialties should be referred to the classification regulations of their specialties.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Mar 07, 2006
- Expiry Date
- Mar 07, 2011
- Cancellation Date
- Nov 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Cardino" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ceb2dfe25b2cdf94fa2baa97297e1e31 and manufactured by CARDINAL HEALTH 200, INC.. The authorized representative in Taiwan is Mitutoyo Medical Equipment Co., Ltd.
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