Bent Rasp 9095.10.162

GUDID 08033390083935

Bent Rasp

LIMACORPORATE SPA

Bone file/rasp, manual, reusable
Primary Device ID08033390083935
NIH Device Record Keyb5d02893-8ab0-4067-b101-9aabebc4b889
Commercial Distribution StatusIn Commercial Distribution
Brand NameBent Rasp
Version Model NumberBent Rasp
Catalog Number9095.10.162
Company DUNS432066322
Company NameLIMACORPORATE SPA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS108033390083935 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWYProsthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08033390083935]

Moist Heat or Steam Sterilization


[08033390083935]

Moist Heat or Steam Sterilization


[08033390083935]

Moist Heat or Steam Sterilization


[08033390083935]

Moist Heat or Steam Sterilization


[08033390083935]

Moist Heat or Steam Sterilization


[08033390083935]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2022-06-10
Device Publish Date2016-08-05

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