Primary Device ID | 10841019107697 |
NIH Device Record Key | 4e2bf69b-ace8-48e8-9302-f7707b3b71a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kirwan |
Version Model Number | 40-1000 |
Company DUNS | 046355210 |
Company Name | KIRWAN SURGICAL PRODUCTS 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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 781-834-9500 |
kprario@ksp.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841019107690 [Primary] |
GS1 | 10841019107697 [Package] Contains: 00841019107690 Package: [5 Units] In Commercial Distribution |
GFA | Blade, Saw, General & Plastic Surgery, Surgical |
Steralize Prior To Use | true |
Device Is Sterile | true |
[10841019107697]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-05-08 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
KIRWAN 75339489 2210573 Live/Registered |
KIRWAN SURGICAL PRODUCTS LLC 1997-08-12 |
KIRWAN 73806454 1629949 Live/Registered |
KIRWAN SURGICAL PRODUCTS, INC. 1989-06-12 |