Primary Device ID | 00853396003533 |
NIH Device Record Key | a5490ce1-38b7-47be-9636-09ae2e60abf3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rumble Tuff |
Version Model Number | PA200DA |
Company DUNS | 067374135 |
Company Name | A CUTE BABY INC |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | true |
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 | 00853396003533 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-27 |
Device Publish Date | 2019-11-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RUMBLE TUFF 86128307 4596010 Live/Registered |
A Cute Baby, Inc 2013-11-25 |
RUMBLE TUFF 75106380 2087311 Live/Registered |
A CUTE BABY, INC. 1996-05-20 |
RUMBLE TUFF 75106380 2087311 Live/Registered |
Peay, Connie B. 1996-05-20 |