Primary Device ID | 00811714030050 |
NIH Device Record Key | ef0b42d5-4afd-4269-a6c3-fa2788cecd49 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Harrier |
Version Model Number | 90-RAA-420100 |
Catalog Number | 90-RAA-420100 |
Company DUNS | 002745858 |
Company Name | RESPONSIVE ORTHOPEDICS LLC |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00811714030050 [Primary] |
MBI | Fastener, Fixation, Nondegradable, Soft Tissue |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-31 |
Device Publish Date | 2019-05-23 |
00811714030067 | Harrier Suture Anchor 5.5mm |
00811714030050 | Harrier Suture Anchor 4.5mm |