Taiwan FDA registration 638ec883a2bac88426258af5650bcd5f
"Heini" laryngoscope and accessory set (unsterilized)
TW: “海尼”喉頭鏡及附件組（未滅菌）
Taiwan·Risk Class 1·HEINE OPTOTECHNIK GMBH & CO. LTD.·Registered Oct 06, 2005 – Oct 06, 2015CancelledRegistration details
- Analysis ID
- 638ec883a2bac88426258af5650bcd5f
- Customs Code
- DHA04400079901
Company information
- Manufacturer
- HEINE OPTOTECHNIK GMBH & CO. LTD.
- Manufacturer Country
- Germany
- Authorized Representative
- SANSOME TRADING CO., LTD.
Product details
- Intended Use
- It is used to examine and examine the patient's upper airway and assist in the placement of endotracheal intubation.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
Dates and status
- Registration Date
- Oct 06, 2005
- Expiry Date
- Oct 06, 2015
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Heini" laryngoscope and accessory set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 638ec883a2bac88426258af5650bcd5f and manufactured by HEINE OPTOTECHNIK GMBH & CO. LTD.. The authorized representative in Taiwan is SANSOME TRADING CO., LTD..
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