MSI
GUDID 00810130206018
769-07 BB Retractor Right (Titanium) UDI 00810130200009
769-12 BB Retractor Left (Titanium) UDI 00810130200016
769-17 BB Retractor Offset (Titanium ) UDI 00810130200023
769-35 Blade Inserting Handle UDI 00810130200047
769-50 BB Blade with Teeth (Titanium) 22.5mm x 34mm UDI 00810130200115
769-51 BB Blade with Teeth (Titanium) 22.5mm x 40mm UDI 00810130200122
769-52 BB Blade with Teeth (Titanium) 22.5mm x 45mm UDI 00810130200139
769-53 BB Blade with Teeth (Titanium) 22.5mm x 50mm UDI 00810130200146
769-54 BB Blade with Teeth (Titanium ) 22.5mm x 55mm UDI 00810130201372
769-55 BB Blade with Teeth (Titanium) 22.5mm x 60mm UDI 00810130200153
769-57 BB Blade with Teeth (Titanium) 22.5mm x 70mm UDI 00810130200160
769-60 BB Blunt Blade (Titanium) 22.5mm x 34mm UDI 00810130200184
769-61 BB Blunt Blade (Titanium) 22.5mm x 40mm UDI 00810130200191
769-62 BB Blunt Blade (Titanium) 22.5mm x 45mm UDI 00810130200207
769-63 BB Blunt Blade (Titanium) 22.5mm x 50mm UDI 00810130200214
769-64 BB Blunt Blade (Titanium) 22.5mm x 55mm UDI 00810130200221
769-65 BB Blunt Blade (Titanium) 22.5mm x 60mm UDI 00810130200238
769-67 BB Blunt Blade (Titanium) 22.5mm x 70mm UDI 00810130200245
769-40 BB Blade with Teeth (Titanium) 26.5mm x 40mm UDI 00810130200252
769-41 BB Blade with Teeth (Titanium) 26.5mm x 47mm UDI 00810130200269
769-42 BB Blade with Teeth (Titanium) 26.5mm x 55mm UDI 00810130200276
769-45 BB Blunt Blade (Titanium) 26.5mm x 40mm UDI 00810130200283
769-46 BB Blunt Blade (Titanium) 26.5mm x 47mm UDI 00810130200290
769-47 BB Blunt Blade (Titanium) 26.5mm x 55mm UDI 00810130200306
968-77 Sterilizing Instrument Case with Lid UDI 00810130200108
Modern Surgical Instruments LLC
Self-retaining surgical retractor, reusable Primary Device ID | 00810130206018 |
NIH Device Record Key | 7ecef3c7-ba63-4bdd-8e07-a2463038a67f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MSI |
Version Model Number | 769-03 |
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 Identifiers
Device Issuing Agency | Device ID |
---|
GS1 | 00810130206018 [Primary] |
FDA Product Code
FFO | Retractor, Self-Retaining |
Sterilization
Steralize Prior To Use | true |
Device Is Sterile | false |
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
[00810130206018]
Moist Heat or Steam Sterilization
Device Entry Metadata
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-04-18 |
Device Publish Date | 2025-04-10 |
On-Brand Devices [MSI]