Transcoject G M B H

FDA Filings

This page includes the latest FDA filings for Transcoject G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number8010803
FEI Number3002655329
NameTRANSCOJECT GMBH
Owner & OperatorTRANSCOJECT GMBH
Contact AddressRUEGENSTRASSE 8 --
NEUMUENSTER DE-SH Schleswig-Holstein 24539 DE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressRUEGENSTRASSE 8
NEUMUENSTER Schleswig-Holstein, 24539 DE
Establishment Type
  • Sterilize Medical Device for Another Party (Contract Sterilizer)
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
TRANSCOJECT GMBH
Cutimed Siltec Sorbact2015-09-01
TRANSCOJECT GMBH
Leukomed range2015-09-01
TRANSCOJECT GMBH
Cutimed Siltec range2015-09-01
TRANSCOJECT GMBH
Double Syringe (ACP) System2015-04-13
TRANSCOJECT GMBH
Transcodent Dental Needle2001-07-27
TRANSCOJECT GMBH
DENTAL NEEDLE2001-07-27

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