Primary Device ID | 07350096321422 |
NIH Device Record Key | 4b9ee665-3011-489b-8a0e-686c6af303d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MulTipeg™ |
Version Model Number | MulTipeg™ 34 |
Catalog Number | 55042 |
Company DUNS | 352736781 |
Company Name | Integration Diagnostics Sweden AB |
Device Count | 1 |
DM Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07350096321422 [Primary] |
EKX | Handpiece, Direct Drive, Ac-Powered |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
[07350096321422]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-09 |
Device Publish Date | 2022-03-01 |