Primary Device ID | 10818087010747 |
NIH Device Record Key | 5cb041a0-6ee4-4ae9-a910-4a695018bb5b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Propper Verline 3/4" Steam Autoclave Tape Mini-Rolls |
Version Model Number | 26814516 |
Catalog Number | 26814516 |
Company DUNS | 001483130 |
Company Name | PROPPER MANUFACTURING COMPANY, INC. |
Device Count | 256 |
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 | 10818087010747 [Unit of Use] |
GS1 | 70818087010749 [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 | 2023-03-03 |
Device Publish Date | 2023-02-23 |
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