Primary Device ID | 00858733006109 |
NIH Device Record Key | 11bb9be5-34b0-4060-82e3-bee8c47b598e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MI Intercostal Retractor System (IRS) 222 Large Blade Set |
Version Model Number | 3.0 |
Catalog Number | MI-IRS-LB-P01 |
Company DUNS | 073724333 |
Company Name | Biorep Technologies, 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 |
---|---|
GS1 | 00858733006109 [Primary] |
DWS | Instruments, Surgical, Cardiovascular |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
[00858733006109]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-01 |
Device Publish Date | 2024-04-23 |
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