| Primary Device ID | 06947656111961 |
| NIH Device Record Key | 73e2c94d-9a01-4302-9057-5946d06c2fa9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AMPMED |
| Version Model Number | AMP1702 |
| Company DUNS | 529391821 |
| Company Name | Guangzhou Berrcom Medical Device Co., Ltd |
| Device Count | 1 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06947656111961 [Primary] |
| FLL | Thermometer, Electronic, Clinical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-12-09 |
| Device Publish Date | 2017-04-17 |
| 06947656112159 | AMP1702 |
| 06947656112142 | AMP1703 |
| 06947656112135 | AMP1703 |
| 06947656112111 | AMP1701 |
| 06947656111961 | AMP1702 |
| 06947656111954 | AMP1701 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() AMPMED 87812567 5575548 Live/Registered |
Amplim LLC 2018-02-27 |