CASTROVIEJO BODY CALIPER 12-9335

GUDID 00192896090279

CASTROVIEJO BODY CALIPER

SONTEC INSTRUMENTS, INC.

Exophthalmometer
Primary Device ID00192896090279
NIH Device Record Keyc33489c7-389a-4c8c-8d51-8bbbe36a4e66
Commercial Distribution StatusIn Commercial Distribution
Brand NameCASTROVIEJO BODY CALIPER
Version Model Number12-9335
Catalog Number12-9335
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896090279 [Primary]

FDA Product Code

HOECaliper, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896090279]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-03
Device Publish Date2018-10-24

On-Brand Devices [CASTROVIEJO BODY CALIPER]

00192896090279CASTROVIEJO BODY CALIPER
00192896090262CASTROVIEJO BODY CALIPER

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