Primary Device ID | 00817330026958 |
NIH Device Record Key | c15470cc-47cc-499a-b795-18f976d50933 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Intrauterine tandem, 20mm, 45ø, titanium |
Version Model Number | AL07366020 |
Catalog Number | AL07366020 |
Company DUNS | 073260622 |
Company Name | MICK RADIO NUCLEAR INSTRUMENT, INC |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
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 | 00817330026958 [Primary] |
JAQ | System, Applicator, Radionuclide, Remote-Controlled |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00817330026958]
Moist Heat or Steam Sterilization
[00817330026958]
Moist Heat or Steam Sterilization
[00817330026958]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-10-14 |