Primary Device ID | 00850144008246 |
NIH Device Record Key | 0e0a4dd1-31df-4f6a-9b73-517bd778ce5e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Getinge Pack Sterilization Roll |
Version Model Number | GUFL7530 |
Catalog Number | 61301606746 |
Company DUNS | 565751992 |
Company Name | PMS TIBBI CIHAZLAR TEKNOLOJISI SANAYI VE TICARET ANONIM SIRKETI |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | 4196935300 |
rdean@lexamed.net |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 70 Percent (%) Relative Humidity |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 70 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850144008239 [Primary] |
GS1 | 00850144008246 [Package] Contains: 00850144008239 Package: Case [8 Units] In Commercial Distribution |
JOJ | Indicator, Physical/Chemical Sterilization Process |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2017-12-17 |
00850144008345 | Sterilization Roll 30cm x 30m |
00850144008321 | Sterilization Roll 23cm x 30m |
00850144008291 | Sterilization Roll 15cm x 30m |
10850144008267 | Sterilization Roll 10cm x 30m |
00850144008246 | Sterilization Roll 7.5cm x 30m |
00850144008215 | Sterilization Roll 5cm x 30m |