DUTAU FORCEPS® 6522

GUDID 14063108108637

Forceps

NOVATECH

Surgical implant handling forceps
Primary Device ID14063108108637
NIH Device Record Keyb868eade-b83a-4644-8dbf-1271d6d75272
Commercial Distribution StatusIn Commercial Distribution
Brand NameDUTAU FORCEPS®
Version Model Number6522
Catalog Number6522
Company DUNS777211640
Company NameNOVATECH
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS114063108108637 [Primary]

FDA Product Code

KAEForceps, Ent

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


[14063108108637]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-19
Device Publish Date2023-06-09

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