I-promelt 39001010

GUDID 04260580283996

Powder, 5kg

S & S Scheftner GmbH

Dental casting non-noble alloy

• Primary Device ID: 04260580283996
• NIH Device Record Key: 09834d1a-a493-4eb7-85a5-8dc839098d40
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: I-promelt
• Version Model Number: 39001010
• Catalog Number: 39001010
• Company DUNS: 321810517
• Company Name: S & S Scheftner 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: true
• 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	04260580283996 [Primary]

FDA Product Code

• EJH: Alloy, Metal, Base

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-16
• Device Publish Date: 2022-05-08

Devices Manufactured by S & S Scheftner GmbH

• 04260207850020 - Starbond Co: 2022-05-16 Ingots, 1000g
• 04260580283972 - Tipladur23: 2022-05-16 Powder, 2.5kg
• 04260580283989 - Fusion AM: 2022-05-16 Powder 45, 5kg
• 04260580283996 - I-promelt: 2022-05-16Powder, 5kg
• 04260580283996 - I-promelt: 2022-05-16 Powder, 5kg
• 04260207850013 - Starbond Ni: 2018-03-29 Ingots, 1000g
• 04260207850037 - Starbond CoS: 2018-03-29 Ingots, 1000g
• 04260207850181 - Modelstar S: 2018-03-29 Ingots, 1000g
• 04260207850198 - Modelstar S: 2018-03-29 Ingots, 250g