HEINE AllSpec® Disposable Tips B-000.11.138

GUDID 04053755191505

Heine Optotechnik GmbH & Co. KG

Ear speculum, single-use
Primary Device ID04053755191505
NIH Device Record Keyfb44d605-d387-46be-bf65-89d888438c95
Commercial Distribution StatusIn Commercial Distribution
Brand NameHEINE AllSpec® Disposable Tips
Version Model Number166
Catalog NumberB-000.11.138
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 Usetrue
Lot Batchfalse
Serial Numberfalse
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(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com
Phone+1(800)643-6275
Emailsupport@midmark.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104053755191505 [Primary]

FDA Product Code

ERAOtoscope

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-06-07
Device Publish Date2017-11-03

On-Brand Devices [HEINE AllSpec® Disposable Tips]

04053755191505166
04053755191499166
04053755191062166
04053755191055166

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