Primary Device ID | 09349221000040 |
NIH Device Record Key | 7fc172bd-72b6-47ae-a9b7-483f68a91905 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medmont Automated Perimeter M700 USB |
Version Model Number | M700 USB |
Company DUNS | 746137249 |
Company Name | MEDMONT INTERNATIONAL PTY LTD |
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 | false |
Serial Number | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09349221000040 [Primary] |
HPT | Perimeter, Automatic, Ac-Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-22 |
Device Publish Date | 2022-09-14 |
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