Primary Device ID | 20814434021197 |
NIH Device Record Key | 77f509ba-8b2e-4f1c-9be8-a79fc1e20934 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Getinge Assured Steam Sterilization Indicator |
Version Model Number | 61301606813 |
Catalog Number | 61301606813 |
Company DUNS | 622223196 |
Company Name | STERITEC PRODUCT MFG. CO., INC. |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814434021193 [Primary] |
GS1 | 10814434021190 [Package] Contains: 00814434021193 Package: Bag [250 Units] In Commercial Distribution |
GS1 | 20814434021197 [Package] Contains: 10814434021190 Package: Case [24 Units] In Commercial Distribution |
LRT | Indicator, Sterilization |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-06-18 |
Device Publish Date | 2019-06-10 |
20814434021203 | 61301606814 |
20814434021197 | 61301606813 |