| 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 |