Primary Device ID | 10078300029851 |
NIH Device Record Key | 6c321ec0-0157-4541-b798-aa665699a798 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OB |
Version Model Number | 02985 |
Company DUNS | 151179769 |
Company Name | EDGEWELL PERSONAL CARE BRANDS, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00078300029854 [Primary] |
GS1 | 10078300029851 [Package] Contains: 00078300029854 Package: [24 Units] In Commercial Distribution |
HEB | TAMPON, MENSTRUAL, UNSCENTED |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-08-05 |
Device Publish Date | 2019-07-26 |
10078300070211 | OB DIG PROC SUP BKA 40 |
10078300070204 | OB DIG PROC REG GK 40 |
20078300070157 | OB DIG PROC MP 40 |
10078300070143 | OB DIG PROC SUP BKA 18 |
10078300070136 | OB DIG PROC REG GK 18 |
10078300070129 | OB DIG HELIX ULTRA DK 40 |
20078300070119 | OB DIG HELIX MP 40 |
20078300070096 | OB DIG HELIX SUP BK 40 |
10078300070082 | OB DIG HELIX REG AL 40 |
20078300070102 | OB DIG HELIX SUP+ CK 40 |
10078300029936 | OB ORGANIC SUP APLC 18ct 4/3 |
10078300029868 | OB ORGANIC REG APLC 18ct 4/3 |
10078300029851 | OB ORGANIC SUP NO APLC 24ct 8/3 |
10078300029837 | OB ORGANIC REG NO APLC 24ct 8/3 |
10078300021794 | 40CT o.b. HELIX ULTRA 4/3 (US/CN) |