Primary Device ID | 10814434021312 |
NIH Device Record Key | 5fd4a423-0953-4930-b4f0-fb3392263e5c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SteriTec Green Tape 1" |
Version Model Number | CI 159/1 |
Catalog Number | CI 159/1 |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814434021315 [Primary] |
GS1 | 10814434021312 [Package] Contains: 00814434021315 Package: Case [36 Units] In Commercial Distribution |
JOJ | Indicator, Physical/Chemical Sterilization Process |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-17 |
Device Publish Date | 2022-06-09 |
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