Primary Device ID | 03760244033598 |
NIH Device Record Key | db70d179-0f3c-4b67-ab8f-7224bafcfe44 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LEKSELL FRAME ADAPTOR |
Version Model Number | 174017-01 |
Catalog Number | ROSAS00348 |
Company DUNS | 264502977 |
Company Name | MEDTECH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
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 | 03760244033598 [Primary] |
HAW | Neurological Stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-07-24 |
Device Publish Date | 2020-06-02 |
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