Primary Device ID | 00816389020221 |
NIH Device Record Key | 4dd68554-4296-4989-badd-e1c9ae70cdc9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kelowna GYN Template for 16 gauge (1.65 mm) needles |
Version Model Number | GM11012210 |
Catalog Number | GM11012210 |
Company DUNS | 332474605 |
Company Name | Varian Medical Systems Deutschland GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 00816389020221 [Primary] |
JAQ | System, applicator, radionuclide, remote-controlled |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
[00816389020221]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-27 |
Device Publish Date | 2024-02-19 |