Coronet

GUDID 05060165012183

COR. Artificial Anterior Chamber

NETWORK MEDICAL PRODUCTS LIMITED

Corneal resection holder, single-use
Primary Device ID05060165012183
NIH Device Record Keya8390788-2d59-44db-abdf-3aa5ceab7815
Commercial Distribution Discontinuation2019-08-27
Commercial Distribution StatusNot in Commercial Distribution
Brand NameCoronet
Version Model Number51-935
Company DUNS458670304
Company NameNETWORK MEDICAL PRODUCTS LIMITED
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS105060165012183 [Primary]

FDA Product Code

HRHTrephine, Manual, Ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-11-27
Device Publish Date2019-08-27

On-Brand Devices [Coronet]

05060165012756Crawford Type Intubation Set
05060165012770Canaliculus Intubation Set
05060165012183COR. Artificial Anterior Chamber

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