Primary Device ID | 00850144008161 |
NIH Device Record Key | 3f5aeea3-7b10-43d0-9692-18606363ef43 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Getinge Pack Tyvek Pouch |
Version Model Number | GUTP2030 |
Catalog Number | 61301606740 |
Company DUNS | 565751992 |
Company Name | PMS TIBBI CIHAZLAR TEKNOLOJISI SANAYI VE TICARET ANONIM SIRKETI |
Device Count | 250 |
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 | 00850144008161 [Primary] |
GS1 | 10850144008168 [Package] Package: Case [4 Units] In Commercial Distribution |
GS1 | 20850144008165 [Unit of Use] |
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 | 2017-10-01 |
00850144008208 | Tyvek Pouch 30cm x 45cm |
00850144008192 | Tyvek Pouch 25cm x 45cm |
00850144008185 | Tyvek Pouch 25cm x 38cm |
00850144008178 | Tyvek Pouch 20cm x 40cm |
00850144008161 | Tyvek Pouch 20cm x 30cm |
00850144008154 | Tyvek Pouch 15cm x 30cm |
00850144008147 | Tyvek Pouch 10cm x 56cm |
00850144008130 | Tyvek Pouch 10cm x 30cm |