Primary Device ID | 20048526069389 |
NIH Device Record Key | 05e43d91-3e3a-4766-87b1-2d377ad4cd76 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nuby |
Version Model Number | 6938 |
Company DUNS | 108926288 |
Company Name | LUV N' CARE, LTD. |
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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | true |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00048526069385 [Primary] |
GS1 | 20048526069389 [Package] Contains: 00048526069385 Package: [4 Units] In Commercial Distribution |
GS1 | 30048526069386 [Package] Package: [12 Units] In Commercial Distribution |
KKO | Ring, Teething, Fluid-Filled |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-03 |
Device Publish Date | 2022-05-26 |