HRT3

GUDID 04059237000266

Heidelberg Engineering GmbH

Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp
Primary Device ID04059237000266
NIH Device Record Key90206e96-4371-403a-afc0-83799679ab37
Commercial Distribution StatusIn Commercial Distribution
Brand NameHRT3
Version Model NumberHRT3 RCM
Company DUNS329833875
Company NameHeidelberg Engineering GmbH
Device Count1
DM Exemptfalse
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 Numbertrue
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
GS104059237000266 [Primary]

FDA Product Code

MXKDevice,Analysis,Anterior Segment

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-02-18
Device Publish Date2016-09-24

On-Brand Devices [HRT3]

04059237000334Rostock Cornea Module SW V1.5a
04059237000273Rostock Cornea Module SW V1.5
04059237000266HRT3 RCM
04059237000730HRT3 RCM

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