MILAGRO 219500

GUDID 10886705023196

MILAGRO ADVANCE Modular Driver

Medos International Sàrl

Surgical screwdriver, reusable

• Primary Device ID: 10886705023196
• NIH Device Record Key: efd013c0-e760-4446-ba5a-d94b65b55de8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MILAGRO
• Version Model Number: 219500
• Catalog Number: 219500
• Company DUNS: 482661753
• Company Name: Medos International Sàrl
• 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

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886705023196 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

[10886705023196]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2025-03-18
• Device Publish Date: 2015-09-01

Devices Manufactured by Medos International Sàrl

• 10886705001507 - GRYPHON: 2025-03-18 GRYPHON OBTURATOR
• 10886705001538 - GRYPHON: 2025-03-18 GRYPHON BLUNT OBTURATOR
• 10886705002634 - RIGIDFIX: 2025-03-18 RIGIDFIX Femoral/Tibial Rod Thumb Screw
• 10886705002993 - RIGIDFIX: 2025-03-18 RIGIDFIX Mallet
• 10886705003440 - NA: 2025-03-18 REUSABLE OBTURATOR 5.5 x 55mm
• 10886705003464 - NA: 2025-03-18 REUSABLE OBTURATOR 5.5 x 75mm
• 10886705003501 - NA: 2025-03-18 REUSABLE OBTURATOR 5.5 x 90mm
• 10886705003525 - NA: 2025-03-18 REUSABLE OBTURATOR 7.0 x 110mm