MU Reverse ScanBody

GUDID 08800266941213

MU Reverse ScanBody (DSMURSBS)

DENTIS CO. ,LTD

Dental implant abutment analog, scanning

• Primary Device ID: 08800266941213
• NIH Device Record Key: 101d3e2c-8fd5-4c24-88af-9fb093e6fed8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MU Reverse ScanBody
• Version Model Number: DSMURSBS
• Company DUNS: 694721181
• Company Name: DENTIS CO. ,LTD
• 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: true
• 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	08800266941213 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

[08800266941213]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-28
• Device Publish Date: 2024-08-20

Devices Manufactured by DENTIS CO. ,LTD

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• 08800053053679 - Aqua Tip: 2024-12-25 Aqua Tip (DSSAT41)
• 08800053064729 - I-FIX Angled Type ScanBody: 2024-11-26 I-FIX Angled Type ScanBody (DFASBS)
• 08800053064736 - I-FIX Angled Type ScanBody: 2024-11-26 I-FIX Angled Type ScanBody (DFASBL)
• 08800053064743 - I-FIX Angled Type ScanBody Screw: 2024-11-26 I-FIX Angled Type ScanBody Screw (DFSBS)
• 08800053064750 - I-FIX Angled Type ScanBody: 2024-11-26 I-FIX Angled Type ScanBody (DFASBSS)
• 08800053064767 - I-FIX Angled Type ScanBody: 2024-11-26 I-FIX Angled Type ScanBody (DFASBLS)
• 08800053093743 - S250 Series(Ceiling, Mobile): 2024-11-07 AC 100-240V, 50/60HZ, 61-94VA