Primary Device ID | 00887482016695 |
NIH Device Record Key | 9b855fb1-d9a6-4491-a0a0-c09863d3b5c4 |
Commercial Distribution Discontinuation | 9999-01-01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Symmetry MEYERDING |
Version Model Number | 50-1191 |
Catalog Number | 50-1191 |
Company DUNS | 079641356 |
Company Name | SYMMETRY SURGICAL INC. |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 |
00887482161005 | Symmetry® Retractor, Meyerding Laminectomy, 25.0 mm X 60.0 mm, 7 in |
00887482160992 | Symmetry® Retractor, Meyerding Laminectomy, 25.0 mm X 30.0 mm, 7 in |
00887482016701 | Symmetry® Retractor, Meyerding, Blade 1 in x 1 3/4 in |
00887482016695 | Symmetry® Retractor, Meyerding, Blade 1 in x 2 in |
00887482016688 | Symmetry® Retractor, Meyerding, Blade 1 in x 2 3/8 in |