Primary Device ID | B3901912101 |
NIH Device Record Key | d6b64a68-4f2d-40fe-bcbd-c72a4ff955b3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reprocessed 4mm EndoScrub Sheath, 30 deg |
Version Model Number | 191210 |
Company DUNS | 785616934 |
Company Name | SURETEK MEDICAL |
Device Count | 1 |
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 | 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 | true |
OTC Over-The-Counter | false |