| 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 |