Primary Device ID | 30841785105822 |
NIH Device Record Key | 520f5521-3c63-473f-8fb2-e576bdde0b1e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Symmetry Olsen |
Version Model Number | 20-5060KI-28 |
Catalog Number | 20-5060KI-28 |
Company DUNS | 079344210 |
Company Name | OLSEN MEDICAL, LLC |
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 | true |
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 | 00841785105821 [Primary] |
GS1 | 30841785105822 [Package] Contains: 00841785105821 Package: [20 Units] In Commercial Distribution |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
[30841785105822]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-12 |