Primary Device ID | 30818087010994 |
NIH Device Record Key | 1190a20d-b4dd-4497-b2e6-c4a6528870e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vapor Line Reusable Process Challenge Device |
Version Model Number | 26906900 |
Catalog Number | 26906900 |
Company DUNS | 001483130 |
Company Name | PROPPER MANUFACTURING COMPANY, 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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 30818087010994 [Primary] |
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 | 2023-06-26 |
Device Publish Date | 2023-06-16 |
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