SYN310.870

GUDID 10888551022941

COUNTERSINK

STERILMED, INC.

Surgical countersink, single-use
Primary Device ID10888551022941
NIH Device Record Keyff030857-4cef-40a5-aaa2-6c942d957ffa
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberSYN310.870
Catalog NumberSYN310.870
Company DUNS175899459
Company NameSTERILMED, 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110888551022941 [Primary]

FDA Product Code

HWWCOUNTERSINK

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10888551022941]

Ethylene Oxide


[10888551022941]

Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-19
Device Publish Date2020-10-09

Devices Manufactured by STERILMED, INC.

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