Primary Device ID | 08057968719491 |
NIH Device Record Key | fd8d3927-0ae3-42a6-b259-fd93b5405df6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRIAL CUP D58 mm |
Version Model Number | 9055.28.458 |
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 | 08057968719491 [Primary] |
HWT | Template |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
Moist Heat or Steam Sterilization
[08057968719491]
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 |
08057968719491 | 9055.28.458 |
08057968712058 | H0030154209 |