Primary Device ID | 10885862295507 |
NIH Device Record Key | b15cef40-81fc-4b25-aec4-f2f4cd39d04c |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 521-50-03 |
Catalog Number | 521-50-03 |
Company DUNS | 157565946 |
Company Name | Exactech, Inc. |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10885862295507 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
[10885862295507]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-05 |
Device Publish Date | 2022-07-28 |
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