Primary Device ID | 00381370051770 |
NIH Device Record Key | d0409aa4-4430-4089-9713-3cd1caf23753 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ELASTIKON |
Version Model Number | 00381370051770 |
Company DUNS | 002347102 |
Company Name | JOHNSON & JOHNSON CONSUMER INC. |
Device Count | 1 |
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 | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(866)565-2873 |
xxx@xxx.com | |
Phone | +1(866)565-2873 |
xxx@xxx.com | |
Phone | +1(866)565-2873 |
xxx@xxx.com | |
Phone | +1(866)565-2873 |
xxx@xxx.com | |
Phone | +1(866)565-2873 |
xxx@xxx.com | |
Phone | +1(866)565-2873 |
xxx@xxx.com | |
Phone | +1(866)565-2873 |
xxx@xxx.com | |
Phone | +1(866)565-2873 |
xxx@xxx.com | |
Phone | +1(866)565-2873 |
xxx@xxx.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00381370051770 [Primary] |
KGX | Tape and bandage, adhesive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2019-01-30 |
00381370051770 | ELASTIKON ELASTIC TAPE 4 Inch X 2.5 Yard |
00381370051718 | ELASTIKON TAPE 3 Inch X 2.5 Yard BULK |
00381370051701 | ELASTIKON TAPE 2 Inch X 2.5 Yard BULK |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ELASTIKON 76669870 3254542 Live/Registered |
JOHNSON & JOHNSON 2006-12-04 |
ELASTIKON 71220027 0208532 Dead/Expired |
JOHNSON & JOHNSON 1925-09-09 |