Primary Device ID | B4195508000 |
NIH Device Record Key | 35c457e2-a45f-43c4-b0b2-376c6493a711 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MSI |
Version Model Number | 55-0800 |
Company DUNS | 118447158 |
Company Name | Modern Surgical Instruments LLC |
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 | B4195508000 [Primary] |
KAE | Forceps, Ent |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
[B4195508000]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-10 |
Device Publish Date | 2022-08-02 |