Primary Device ID | 10815634020686 |
NIH Device Record Key | ccb904c5-1947-4572-8c0f-f49673bdfc55 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arthrex BioExpress |
Version Model Number | ABS-10053-15 |
Company DUNS | 066839630 |
Company Name | MICROMEDICS, 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815634020689 [Primary] |
GS1 | 10815634020686 [Package] Contains: 00815634020689 Package: Inner Pack [5 Units] In Commercial Distribution |
GS1 | 20815634020683 [Package] Package: Case [1 Units] In Commercial Distribution |
FMF | Syringe, Piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-03 |
Device Publish Date | 2021-04-25 |
10815634020709 | GD-1115-150 with 45 degree custom cannula |
10815634020693 | GD-1115-100 with 45 degree custom cannula |
10815634020686 | Graft Delivery Device |
10815634020334 | Graft Delivery Device |