Primary Device ID | 00070048021657 |
NIH Device Record Key | ea6469d4-7fe4-4bcf-9e55-ab1dde27e16f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Goo Gone Bandage & Adhesive Remover |
Version Model Number | PKT |
Company DUNS | 080214481 |
Company Name | MICRO-SCIENTIFIC, LLC |
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 | 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 | 00070048021657 [Primary] |
GS1 | 00070048221651 [Package] Package: shrink wrap [2 Units] In Commercial Distribution |
GS1 | 10070048021654 [Package] Package: carton [12 Units] In Commercial Distribution |
KOX | Solvent, Adhesive Tape |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-31 |
Device Publish Date | 2022-08-23 |
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