Primary Device ID | B16556440326083124108 |
NIH Device Record Key | 9cda6dcf-9134-4ee0-8509-b9e0aeb95d95 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Implant Needle |
Version Model Number | 5644 |
Company DUNS | 967592978 |
Company Name | Liberty 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 | 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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B16556440326083124108 [Primary] |
IWJ | System, Applicator, Radionuclide, Manual |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-29 |
Device Publish Date | 2024-08-21 |
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B16556440326083124108 | 17ga 20cm Implant needle-1/pk |
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