Primary Device ID | 24053613284381 |
NIH Device Record Key | bf442f5c-9de2-42cf-9609-cbff97d74521 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GUIDE PIN SET |
Version Model Number | OC04N.127.032 |
Catalog Number | OC04N.127.032 STE |
Company DUNS | 317409001 |
Company Name | Gebr. Brasseler GmbH & Co. KG |
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 | true |
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 |