Primary Device ID | 10861887000210 |
NIH Device Record Key | 641f41c8-2716-415c-b629-5f9ae90109c7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INRO Surgical Nail |
Version Model Number | 00-4R |
Catalog Number | 4R |
Company DUNS | 623674272 |
Company Name | Inro Medical Designs 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 | true |
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 |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com | |
Phone | 1 800 527 1093 |
info@inro.com |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Width | 14 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00861887000213 [Primary] |
GS1 | 10861887000210 [Package] Contains: 00861887000213 Package: form filled seal [1 Units] Discontinued: 2024-12-31 In Commercial Distribution |
FYH | Splint, Extremity, Noninflatable, External, Sterile |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-25 |
Device Publish Date | 2023-08-17 |