Large Staple Punch

GUDID M209176530

BIOPRO, INC.

Bone awl
Primary Device IDM209176530
NIH Device Record Key10ec4d6c-a3ff-47eb-9ce3-b6c6d3768773
Commercial Distribution StatusIn Commercial Distribution
Brand NameLarge Staple Punch
Version Model Number17653
Company DUNS618749857
Company NameBIOPRO, INC.
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM209176530 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWJAwl

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M209176530]

Moist Heat or Steam Sterilization


[M209176530]

Moist Heat or Steam Sterilization


[M209176530]

Moist Heat or Steam Sterilization


[M209176530]

Moist Heat or Steam Sterilization


[M209176530]

Moist Heat or Steam Sterilization


[M209176530]

Moist Heat or Steam Sterilization


[M209176530]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-05-09
Device Publish Date2019-05-01

On-Brand Devices [Large Staple Punch]

M20917653017653
0081001248382717653

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