Eckardt temporary keratoprosthesis, Ø 7 mm, 2.8 mm depth 1285.1

GUDID 08717872004532

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Therapeutic contact lens
Primary Device ID08717872004532
NIH Device Record Keyb271b797-3d6d-44e3-a91d-1cccb65dabe0
Commercial Distribution StatusIn Commercial Distribution
Brand NameEckardt temporary keratoprosthesis, Ø 7 mm, 2.8 mm depth
Version Model Number1285.1
Catalog Number1285.1
Company DUNS407522184
Company NameD.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108717872004532 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MLPKeratoprosthesis, Temporary Implant, Surgical Use

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08717872004532]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-05-08
Device Publish Date2016-09-23

Devices Manufactured by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

18717872034710 - CUSTOM TDC VITREC.PACK VGP 25G2024-10-07
18717872034932 - 23G High Flow infusion line2024-02-29
18717872034949 - 25G High Flow infusion line2024-02-29
18717872034956 - 27G High Flow infusion line2024-02-29
18717872035106 - EVA NEXUS™ Posterior 23G TDC Pack2024-02-29
18717872035113 - EVA NEXUS™ Posterior 25G TDC Pack2024-02-29
18717872035120 - EVA NEXUS™ Posterior 27G TDC Pack2024-02-29
18717872035304 - EVA NEXUS™ Posterior 23G TDC Pack2024-02-29

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.