Primary Device ID | M263ABS30001 |
NIH Device Record Key | 0a417dc0-b430-4771-b30c-a93f33c3e275 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arthrex DX Reinforcement Matrix |
Version Model Number | 30030-01 |
Catalog Number | ABS-30001S |
Company DUNS | 131107757 |
Company Name | DSM BIOMEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M263ABS30001 [Primary] |
OWY | Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2022-06-10 |
Device Publish Date | 2015-09-04 |
00812337020022 | 30030-02 |
00812337020015 | 30030-01 |
M263ABS30002 | 30030-02 |
M263ABS30001 | 30030-01 |