| Primary Device ID | 20813172023906 |
| NIH Device Record Key | 057eee0f-86c5-4c4e-a36f-d92f54b9f41a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NitriDerm® 800 |
| Version Model Number | 118300 |
| Company DUNS | 802020693 |
| Company Name | INNOVATIVE HEALTHCARE CORPORATION |
| Device Count | 50 |
| 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 | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813172023902 [Unit of Use] |
| GS1 | 10813172023909 [Primary] |
| GS1 | 20813172023906 [Package] Contains: 10813172023909 Package: 50 pr/bag, 4 bags/cs [4 Units] In Commercial Distribution |
| LZC | Patient Examination Glove, Specialty |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2025-02-24 |
| Device Publish Date | 2022-12-08 |
| 20813172023913 | Gloves, Exam, Nitrile, Sterile, Chemo, Powder-Free, Pairs, Extended Cuff, USP 797/800, XL |
| 20813172023906 | Gloves, Exam, Nitrile, Sterile, Chemo, Powder-Free, Pairs, Extended Cuff, USP 797/800, L |
| 00813172023896 | Gloves, Exam, Nitrile, Sterile, Chemo, Powder-Free, Pairs, Extended Cuff, USP 797/800, M |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NITRIDERM 75645079 2449807 Live/Registered |
Innovative Healthcare Supply, Inc. 1999-02-23 |