234-020-093

GUDID 04546540755902

SEMI-T STRIPPER

STRYKER CORPORATION

Tendon stripper
Primary Device ID04546540755902
NIH Device Record Key1f2afc4d-68d8-4983-87ce-5e0409dec11c
Commercial Distribution StatusIn Commercial Distribution
Version Model Number234-020-093
Catalog Number234-020-093
Company DUNS187502109
Company NameSTRYKER CORPORATION
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(866)624-4422
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS104546540755902 [Primary]

FDA Product Code

HRTSTRIPPER, SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04546540755902]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-09-04

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