BETA 200 LED RETINOSCOPE C-008.15.353

GUDID 04053755191673

3,5 V

Heine Optotechnik GmbH & Co. KG

Retinoscope, battery-powered
Primary Device ID04053755191673
NIH Device Record Keyae00e680-189a-4260-9edc-64d014442b90
Commercial Distribution StatusIn Commercial Distribution
Brand NameBETA 200 LED RETINOSCOPE
Version Model Number000
Catalog NumberC-008.15.353
Company DUNS315274563
Company NameHeine Optotechnik GmbH & Co. KG
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104053755191598 [Package]
Package: Carton [1 Units]
In Commercial Distribution
GS104053755191673 [Primary]

FDA Product Code

HKMRetinoscope, Battery-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2024-07-17
Device Publish Date2022-12-12

On-Brand Devices [BETA 200 LED RETINOSCOPE]

040537551916733,5 V
040537552025082,5 V

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