Arthrex DX Reinforcement Matrix ABS-30001S

GUDID M263ABS30001

DSM BIOMEDICAL, INC.

Extra-gynaecological surgical mesh, collagen, bioabsorbable
Primary Device IDM263ABS30001
NIH Device Record Key0a417dc0-b430-4771-b30c-a93f33c3e275
Commercial Distribution StatusIn Commercial Distribution
Brand NameArthrex DX Reinforcement Matrix
Version Model Number30030-01
Catalog NumberABS-30001S
Company DUNS131107757
Company NameDSM BIOMEDICAL, 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 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

Device Dimensions

Length5 Centimeter
Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
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Width5 Centimeter
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Width5 Centimeter
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Width5 Centimeter
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Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
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Width5 Centimeter
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Width5 Centimeter
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Length5 Centimeter
Width5 Centimeter
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Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
Length5 Centimeter
Width5 Centimeter
Length5 Centimeter
Width5 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM263ABS30001 [Primary]

FDA Product Code

OWYMesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-06-10
Device Publish Date2015-09-04

On-Brand Devices [Arthrex DX Reinforcement Matrix ]

0081233702002230030-02
0081233702001530030-01
M263ABS3000230030-02
M263ABS3000130030-01

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