XIA II 48040100

GUDID 07613327262889

ROD ROTATION FORCEPS

Stryker Corporation

Surgical implant handling forceps
Primary Device ID07613327262889
NIH Device Record Keyb3b020e5-d184-40c2-ae03-36d7d1e3da0e
Commercial Distribution Discontinuation2025-03-17
Commercial Distribution StatusIn Commercial Distribution
Brand NameXIA II
Version Model Number48040100
Catalog Number48040100
Company DUNS149183167
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327262889 [Primary]

FDA Product Code

HAOINSTRUMENT, SURGICAL, NON-POWERED

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613327262889]

Moist Heat or Steam Sterilization


[07613327262889]

Moist Heat or Steam Sterilization


[07613327262889]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2025-03-10
Device Publish Date2019-11-21

On-Brand Devices [XIA II]

07613154407996POLYAXIAL REDUCTION SCREW
07613154407989POLYAXIAL REDUCTION SCREW
07613154407972POLYAXIAL REDUCTION SCREW
07613154407965POLYAXIAL REDUCTION SCREW
07613154407958POLYAXIAL REDUCTION SCREW
07613154407941POLYAXIAL REDUCTION SCREW
07613154407934POLYAXIAL REDUCTION SCREW
07613154407927POLYAXIAL REDUCTION SCREW
07613154407910POLYAXIAL REDUCTION SCREW
07613154407903POLYAXIAL REDUCTION SCREW
07613154407897POLYAXIAL REDUCTION SCREW
07613154407880POLYAXIAL REDUCTION SCREW
07613154407873POLYAXIAL REDUCTION SCREW
07613154407866POLYAXIAL REDUCTION SCREW
07613154407859POLYAXIAL REDUCTION SCREW
07613154407842POLYAXIAL REDUCTION SCREW
07613154407835POLYAXIAL REDUCTION SCREW
07613154407828POLYAXIAL REDUCTION SCREW
07613154407811POLYAXIAL REDUCTION SCREW
07613154407804POLYAXIAL REDUCTION SCREW
07613154407798POLYAXIAL REDUCTION SCREW
07613154407781POLYAXIAL REDUCTION SCREW
07613154407774POLYAXIAL REDUCTION SCREW
07613154407767POLYAXIAL REDUCTION SCREW
07613154407750POLYAXIAL REDUCTION SCREW
07613154407743MONOAXIAL REDUCTION SCREW
07613154407736MONOAXIAL REDUCTION SCREW
07613154407729MONOAXIAL REDUCTION SCREW
07613154407712MONOAXIAL REDUCTION SCREW
07613154407705MONOAXIAL REDUCTION SCREW
07613154407699MONOAXIAL REDUCTION SCREW
07613154407682MONOAXIAL REDUCTION SCREW
07613154407675MONOAXIAL REDUCTION SCREW
07613154407668MONOAXIAL REDUCTION SCREW
07613154407651MONOAXIAL REDUCTION SCREW
07613154407644MONOAXIAL REDUCTION SCREW
07613154407637MONOAXIAL REDUCTION SCREW
07613154407620MONOAXIAL REDUCTION SCREW
07613154407613MONOAXIAL REDUCTION SCREW
07613154407606MONOAXIAL REDUCTION SCREW
07613154407590MONOAXIAL REDUCTION SCREW
07613154407583MONOAXIAL REDUCTION SCREW
07613154407576MONOAXIAL REDUCTION SCREW
07613154407569MONOAXIAL REDUCTION SCREW
07613154407552MONOAXIAL REDUCTION SCREW
07613154407545MONOAXIAL REDUCTION SCREW
07613154407538MONOAXIAL REDUCTION SCREW
07613154407521MONOAXIAL REDUCTION SCREW
07613154407514MONOAXIAL REDUCTION SCREW
07613154407507MONOAXIAL REDUCTION SCREW

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.