| Primary Device ID | 20817583020516 |
| NIH Device Record Key | 16f132ea-e223-41b5-899e-5cd213206a31 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Combo |
| Version Model Number | SHI5194T |
| Catalog Number | SHI5194T |
| Company DUNS | 003687733 |
| Company Name | ALPHA PRO TECH INC |
| Device Count | 25 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 520-281-0127 |
| XX@XX.XX | |
| Phone | 1-520-281-0127 |
| XX@XX.XX | |
| Phone | 1-520-281-0127 |
| XX@XX.XX | |
| Phone | 1-520-281-0127 |
| XX@XX.XX | |
| Phone | 1-520-281-0127 |
| XX@XX.XX | |
| Phone | 1-520-281-0127 |
| XX@XX.XX | |
| Phone | 1-520-281-0127 |
| XX@XX.XX | |
| Phone | 1-520-281-0127 |
| XX@XX.XX | |
| Phone | 1-520-281-0127 |
| XX@XX.XX |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817583020512 [Unit of Use] |
| GS1 | 10817583020519 [Primary] |
| GS1 | 20817583020516 [Package] Contains: 10817583020519 Package: CASE [4 Units] In Commercial Distribution |
| FXX | Mask, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-05-06 |
| Device Publish Date | 2016-11-03 |
| 20817583020516 | TIE MASK W/ SNAP ON SHIELD, BLUE 7 MIL. |
| 20817583020509 | EARLOOP MASKW/SHIELD AND SNAPS, BLUE 7 MIL. |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() COMBO 98400376 not registered Live/Pending |
Saunders Archery Company 2024-02-09 |
![]() COMBO 88421475 not registered Live/Pending |
Combo Office, Inc. 2019-05-08 |
![]() COMBO 88341716 not registered Live/Pending |
ORBUSNEICH MEDICAL PTE. LTD. 2019-03-15 |
![]() COMBO 88058303 not registered Live/Pending |
American Biosystems, Inc 2018-07-30 |
![]() COMBO 86869627 not registered Dead/Abandoned |
ORBUSNEICH MEDICAL PTE. LTD. 2016-01-08 |
![]() COMBO 86604293 not registered Dead/Abandoned |
ORBUSNEICH MEDICAL PTE. LTD. 2015-04-21 |
![]() COMBO 86354314 5105463 Live/Registered |
ORBUSNEICH MEDICAL PTE. LTD. 2014-07-31 |
![]() COMBO 86159633 4800445 Live/Registered |
Camp Scandinavia AB 2014-01-07 |
![]() COMBO 85982593 not registered Dead/Abandoned |
OrbusNeich Medical, Inc. 2013-04-27 |
![]() COMBO 85916712 not registered Dead/Abandoned |
OrbusNeich Medical, Inc. 2013-04-27 |
![]() COMBO 85815426 not registered Dead/Abandoned |
Metropolitan Life Insurance Company 2013-01-04 |
![]() COMBO 85635677 4455883 Live/Registered |
Roche Diagnostics GmbH 2012-05-25 |