| Primary Device ID | 08057968712003 |
| NIH Device Record Key | 051094c7-e8b9-426e-90b0-8f784ba8a671 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TRIAL CUP D48 mm |
| Version Model Number | H0030152209 |
| Company DUNS | 895802853 |
| Company Name | HPF SRL |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08057968712003 [Primary] |
| HWT | Template |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
[08057968712003]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-19 |
| Device Publish Date | 2022-09-09 |
| 08057968719392 | 9055.28.448 |
| 08057968712003 | H0030152209 |