Primary Device ID | 00853799007138 |
NIH Device Record Key | 054e7283-2c38-49c6-ab98-d3a1f42a4e6b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Full Length 088 x 132cm Access System |
Version Model Number | FD 1185 |
Catalog Number | REF 4002 |
Company DUNS | 067429673 |
Company Name | ROUTE 92 MEDICAL |
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 | true |
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 |
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