Primary Device ID | B12895010 |
NIH Device Record Key | 6cc8a5f3-e0dd-4a33-8063-a4029d12f6e8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | YOKE, CGA-950 X CGA-346 MALE |
Version Model Number | 9501 |
Catalog Number | 9501 |
Company DUNS | 095472262 |
Company Name | Bay Corporation |
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 | 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 | true |
OTC Over-The-Counter | false |
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