Primary Device ID | 10818087010488 |
NIH Device Record Key | 45d5b9d6-fd99-4900-816c-d08fdcd1155d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Carbon Surgical Blades Sterile #20 |
Version Model Number | 12202000 |
Catalog Number | 12202000 |
Company DUNS | 001483130 |
Company Name | PROPPER MANUFACTURING COMPANY, INC. |
Device Count | 150 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 | 10818087010488 [Unit of Use] |
GS1 | 30818087010482 [Primary] |
GES | Blade, Scalpel |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-16 |
Device Publish Date | 2020-03-06 |
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