CEREC MTL Zirconia

GUDID J01753654500260

CEREC MTL Zirconia, B1, medi, 2 pcs. (5365450026)

Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft

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• Primary Device ID: J01753654500260
• NIH Device Record Key: 9a0abf70-6b8d-469f-808a-0b55da890b12
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CEREC MTL Zirconia
• Version Model Number: 5365450026
• Company DUNS: 315165357
• Company Name: Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft
• 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: 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

Customer Support Contacts

• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	J01753654500260 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180703

FDA Product Code

• EIH: POWDER, PORCELAIN

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-05-10
• Device Publish Date: 2021-04-19

On-Brand Devices [CEREC MTL Zirconia]

• J01753654500370: CEREC MTL Zirconia, BL1, medi, 2 pcs. (5365450037)
• J01753654500340: CEREC MTL Zirconia, D2, medi, 2 pcs. (5365450034)
• J01753654500310: CEREC MTL Zirconia, C2, medi, 2 pcs. (5365450031)
• J01753654500270: CEREC MTL Zirconia, B2, medi, 2 pcs. (5365450027)
• J01753654500260: CEREC MTL Zirconia, B1, medi, 2 pcs. (5365450026)
• J01753654500240: CEREC MTL Zirconia, A3.5, medi, 2 pcs. (5365450024)
• J01753654500230: CEREC MTL Zirconia, A3, medi, 2 pcs. (5365450023)
• J01753654500220: CEREC MTL Zirconia, A2, medi, 2 pcs. (5365450022)
• J01753654500210: CEREC MTL Zirconia, A1, medi, 2 pcs. (5365450021)
• J01753654500170: CEREC MTL Zirconia, BL1, mono, 4 pcs. (5365450017)
• J01753654500140: CEREC MTL Zirconia, D2, mono, 4 pcs. (5365450014)
• J01753654500110: CEREC MTL Zirconia, C2, mono, 4 pcs. (5365450011)
• J01753654500070: CEREC MTL Zirconia, B2, mono, 4 pcs. (5365450007)
• J01753654500060: CEREC MTL Zirconia, B1, mono, 4 pcs. (5365450006)
• J01753654500040: CEREC MTL Zirconia, A3.5, mono, 4 pcs. (5365450004)
• J01753654500030: CEREC MTL Zirconia, A3, mono, 4 pcs. (5365450003)
• J01753654500020: CEREC MTL Zirconia, A2, mono, 4 pcs. (5365450002)
• J01753654500010: CEREC MTL Zirconia, A1, mono, 4 pcs. (5365450001)