Pectus Bar Template, 305 mm 021-12305

GUDID 04260029580280

MedXpert GmbH

Surgical implant template, reusable

• Primary Device ID: 04260029580280
• NIH Device Record Key: 74749a7e-e07e-4cec-8d09-532445706eb4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pectus Bar Template, 305 mm
• Version Model Number: 021-12305
• Catalog Number: 021-12305
• Company DUNS: 331019344
• Company Name: MedXpert GmbH
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +4976345085630
• Email: ask-the-xpert@medXpert.de

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260029580280 [Primary]

FDA Product Code

• MDM: Instrument, Manual, Surgical, General Use

Sterilization

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

[04260029580280]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-06-26
• Device Publish Date: 2017-01-09

Devices Manufactured by MedXpert GmbH

• 04260029583298 - Sternum Repositioning Forceps: 2019-03-21
• 04260029584714 - Pectus screwdriver: 2018-10-05
• 04260029586565 - Pectus Bar Stabilizer, Universal, R, 2 x Ø4x8 mm: 2018-08-10
• 04260029586572 - Pectus Bar Stabilizer, Universal, L, 2 x Ø4x8 mm: 2018-08-10
• 04260029580204 - Pectus Allergy Test Plate: 2018-06-26
• 04260029580235 - Pectus Bar Template, 178 mm: 2018-06-26
• 04260029580242 - Pectus Bar Template, 203 mm: 2018-06-26
• 04260029580259 - Pectus Bar Template, 229 mm: 2018-06-26