Primary Device ID | 00850144008093 |
NIH Device Record Key | e984b329-bfc2-4f41-8a44-3bb0db0ce224 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Getinge Pack Tyvek Roll |
Version Model Number | GUTY1030 |
Catalog Number | 61301606733 |
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 Temperature | Between 0 Degrees Celsius and 35 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 35 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850144008093 [Primary] |
GS1 | 10850144008090 [Package] Package: Case [6 Units] In Commercial Distribution |
FRG | Wrap, Sterilization |
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 | 2017-09-25 |
10850144008120 | Tyvek Roll 25cm x 30m |
00850144008116 | Tyvek Roll 20cm x 30m |
00850144008109 | Tyvek Roll 15cm x 30m |
00850144008093 | Tyvek Roll 10cm x 30m |
10850144008083 | Tyvek Roll 05cm x 30m |