Primary Device ID | 60017276238640 |
NIH Device Record Key | d38659a0-0019-44b2-b20a-da269a196ac5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dreamworks Gabby's Dollhouse |
Version Model Number | 017276238648 |
Company DUNS | 152793493 |
Company Name | Aso LLC |
Device Count | 14 |
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 | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00017276238648 [Primary] |
GS1 | 60017276238640 [Unit of Use] |
KGX | Tape And Bandage, Adhesive |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-01-19 |
Device Publish Date | 2022-01-11 |