Primary Device ID | G586903113A0 |
NIH Device Record Key | 7e5f1350-963e-4035-bf4f-34b458ca36cb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Novosurgical |
Version Model Number | 9031-13A |
Company DUNS | 033029433 |
Company Name | NOVO SURGICAL, 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 | 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 |
---|---|
HIBCC | G586903113A0 [Primary] |
GDO | Applier, Surgical, Clip |
Steralize Prior To Use | true |
Device Is Sterile | false |
[G586903113A0]
Moist Heat or Steam Sterilization
[G586903113A0]
Moist Heat or Steam Sterilization
[G586903113A0]
Moist Heat or Steam Sterilization
[G586903113A0]
Moist Heat or Steam Sterilization
[G586903113A0]
Moist Heat or Steam Sterilization
[G586903113A0]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-23 |
Device Publish Date | 2024-12-13 |
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