DELTA 30 K-230.28.305

GUDID 04053755197187

Heine Optotechnik GmbH & Co. KG

Dermatoscope, optical
Primary Device ID04053755197187
NIH Device Record Key2291a275-14f2-4fb8-b2dd-939b8abf8212
Commercial Distribution StatusIn Commercial Distribution
Brand NameDELTA 30
Version Model Number083
Catalog NumberK-230.28.305
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com
Phone+4908152380
Emailinfo@heine.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104053755197187 [Primary]

FDA Product Code

KYTLight, Examination, Medical, Battery Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-29
Device Publish Date2020-01-21

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04053755186556 - BETA 200 LED VET. OTOSCOPE2024-07-05
04053755202133 - K180 LED F.O. OTOSCOPE 2024-07-05
04053755202232 - K 180 LED OPHTHALMOSCOPE2024-07-05

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