Primary Device ID | 00847538007855 |
NIH Device Record Key | 3578939b-2402-4a8a-9c1c-76d7d47627d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reverse Curette, 11mm |
Version Model Number | 10-055-400 |
Catalog Number | 2709-01-011 |
Company DUNS | 079881212 |
Company Name | SYMMETRY MEDICAL INC. |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00847538007855 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00847538007855]
Moist Heat or Steam Sterilization
[00847538007855]
Moist Heat or Steam Sterilization
[00847538007855]
Moist Heat or Steam Sterilization
[00847538007855]
Moist Heat or Steam Sterilization
[00847538007855]
Moist Heat or Steam Sterilization
[00847538007855]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-20 |
Device Publish Date | 2022-05-12 |
00847538007855 | Reverse Curette, 11mm |
00847538001273 | Reverse Curette, 11mm |