Primary Device ID | 04719880260034 |
NIH Device Record Key | c3c4a973-30f5-436a-8657-2af3d385c342 |
Commercial Distribution Discontinuation | 2023-07-26 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ANGELINE |
Version Model Number | RIGL2 |
Company DUNS | 656231540 |
Company Name | ANGELINE GROUP LTD. |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04719880260034 [Primary] |
GS1 | 04719880260041 [Package] Package: Polybag [12 Units] Discontinued: 2023-07-23 In Commercial Distribution |
GS1 | 14719880260048 [Package] Package: CASE [60 Units] Discontinued: 2023-07-23 In Commercial Distribution |
OEA | Non-Surgical Isolation Gown |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-20 |
Device Publish Date | 2020-08-12 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ANGELINE 90225972 not registered Live/Pending |
America Hermax Co.,Limited. 2020-09-30 |
ANGELINE 85381999 4231023 Live/Registered |
AS IP Holdco, LLC 2011-07-27 |
ANGELINE 78490071 3130931 Dead/Cancelled |
Ty Inc. 2004-09-27 |
ANGELINE 76162168 not registered Dead/Abandoned |
de Meester, Angeline M. 2000-11-08 |
ANGELINE 74601541 1931580 Live/Registered |
MARTIN RAY WINERY, INC. 1994-11-21 |