| Primary Device ID | 07350096322221 |
| NIH Device Record Key | d38693e1-d837-47af-a552-6cbeee344789 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MulTipeg™ |
| Version Model Number | MulTipeg™ 102 |
| Catalog Number | 55136 |
| 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 | 07350096322221 [Primary] |
| EKX | Handpiece, Direct Drive, Ac-Powered |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
[07350096322221]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-03-16 |
| Device Publish Date | 2022-03-08 |