| Primary Device ID | 00812594011603 |
| NIH Device Record Key | 703072ba-c663-41e3-9238-f6517e497bb9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NeoBond |
| Version Model Number | 10812594011600 |
| Catalog Number | N742 |
| Company DUNS | 198013435 |
| Company Name | NEOTECH PRODUCTS, INC. |
| Device Count | 15 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812594011603 [Unit of Use] |
| GS1 | 10812594011600 [Primary] |
| KGX | Tape And Bandage, Adhesive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-06-23 |
| Device Publish Date | 2021-06-15 |
| 00812594011603 | Hydrocolloid Roll - 1" x 15' Roll |
| 00812594010330 | Hydrocolloid Strip |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEOBOND 90298752 not registered Live/Pending |
Halliburton Energy Services, Inc. 2020-11-04 |
![]() NEOBOND 79109170 4223884 Dead/Cancelled |
Aleksandrs Gutmans 2011-12-22 |
![]() NEOBOND 78702388 3123723 Live/Registered |
DENTSPLY SIRONA INC. 2005-08-29 |
![]() NEOBOND 75516937 2363108 Live/Registered |
NEOTECH PRODUCTS LLC 1998-07-10 |