REFLECTYS SRTYS-B3

GUDID 03760260220071

ITENA CLINICAL

Dental composite resin

• Primary Device ID: 03760260220071
• NIH Device Record Key: 7fa161da-b862-4607-9e05-c974dc02d700
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REFLECTYS
• Version Model Number: B3
• Catalog Number: SRTYS-B3
• Company DUNS: 278261221
• Company Name: ITENA CLINICAL
• 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: true
• 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	03760260220071 [Primary]

FDA Product Code

• EBF: Material, Tooth Shade, Resin

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-11-10
• Device Publish Date: 2016-10-15

On-Brand Devices [REFLECTYS]

• 03760260220316: P CP
• 03760260220309: I CP
• 03760260220293: E CP
• 03760260220286: A3O CP
• 03760260220279: A2O CP
• 03760260220262: D3 CP
• 03760260220255: C3 CP
• 03760260220248: C2 CP
• 03760260220231: B3 CP
• 03760260220224: B2 CP
• 03760260220217: B1 CP
• 03760260220200: A4 CP
• 03760260220194: A3.5 CP
• 03760260220187: A3 CP
• 03760260220170: A2 CP
• 03760260220163: A1 CP
• 03760260220156: P
• 03760260220149: I
• 03760260220132: E
• 03760260220125: A30
• 03760260220118: A20
• 03760260220101: D3
• 03760260220095: C3
• 03760260220088: C2
• 03760260220071: B3
• 03760260220064: B2
• 03760260220057: B1
• 03760260220040: A4
• 03760260220033: A3.5
• 03760260220026: A3
• 03760260220019: A2
• 03760260220002: A1