MODUS M-6726

GUDID 07630037814900

Lid f. Implant and Instr.Case 120x240mm

Medartis AG

Sterilization/disinfection container Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable

• Primary Device ID: 07630037814900
• NIH Device Record Key: 7731e384-fa72-4067-8db6-8ba405ae9bc4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MODUS
• Version Model Number: M-6726
• Catalog Number: M-6726
• Company DUNS: 480054895
• Company Name: Medartis AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	07630037814900 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193554

FDA Product Code

• HRS: Plate, Fixation, Bone

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

[07630037814900]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-27
• Device Publish Date: 2020-04-17

On-Brand Devices [MODUS]

• 07630037814917: Lid f. Implant and Instr.Case 240x240mm
• 07630037814900: Lid f. Implant and Instr.Case 120x240mm
• 07630037850380: Holding Rack f. Implant and Instr. Cases
• 07630037814894: Implant and Instrument Case 240x54mm
• 07630037814887: Implant and Instrument Case 240x37mm
• 07630037814863: Implant and Instrument Case 120x54mm
• 07630037814856: Implant and Instrument Case 120x37mm
• 07630008491451: Holding Rack f.Case,240x240mm,Height7-12
• 07630008439927: Holding Rack f. Implant and Instr. Cases
• 07630037856320: Lid f. Implant and Instr.Case 240x240mm
• 07630037856313: Lid f. Implant and Instr.Case 120x240mm
• 07630037850373: Lid f. Implant and Instr.Case 240x240mm
• 07630037850366: Lid f. Implant and Instr.Case 120x240mm
• 07630037850151: Lid for Instrument Case M-6320
• 07630894806223: Lid f. Implant and Instr.Case 240x240mm
• 07630894806209: Lid f. Implant and Instr.Case 120x240mm
• 07630894806186: Holding Rack f.Case,240x240mm,Height7-12
• 07630894806162: Holding Rack f. Implant and Instr. Cases
• 07630894806148: Lid f. Implant and Instr.Case 240x240mm
• 07630894806070: Lid for Instrument Case M-6320
• 07630037874584: 1.5 Screwdriver Blade, HD4, 69mm
• 07630037874492: 1.5 ScrewdriverBl.,Cross,Self-Hold.,69mm
• 07630037866398: Titanium Trauma Splint, 100 x 0.2mm
• 07630037866381: Titanium Trauma Splint, 52 x 0.2mm
• 07630037856269: Implant and Instrument Case 120 x 20 mm
• 07630894808319: 2.2 CCS Short Thread 46/09mm, 1/Pkg