Primary Device ID | B268L274120 |
NIH Device Record Key | 46d1a14b-7203-4d10-b879-2747a802515f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LAMAZE/JOHN DEERE |
Version Model Number | L27412 |
Catalog Number | L27412 |
Company DUNS | 065183758 |
Company Name | TOMY INTERNATIONAL, 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 | 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 | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B268L274120 [Primary] |
HIBCC | B268L274122 [Package] Package: Retail Package [2 Units] In Commercial Distribution |
HIBCC | B268L274128 [Package] Contains: B268L274122 Package: Inner Carton [4 Units] In Commercial Distribution |
HIBCC | B268L274129 [Package] Contains: B268L274128 Package: Master Carton [3 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 | 2019-10-01 |
Device Publish Date | 2019-09-23 |
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