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 |