Quinelato QD.153.00

GUDID 07898506845392

Minnesota Cawood retractor

Schobell Industrial Ltda

Hand-held dental retractor

• Primary Device ID: 07898506845392
• NIH Device Record Key: 3a6bced7-349e-4735-8fd1-e13f67acdc2c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Quinelato
• Version Model Number: QD.153.00
• Catalog Number: QD.153.00
• Company DUNS: 899060826
• Company Name: Schobell Industrial Ltda
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07898506845392 [Primary]

FDA Product Code

• EIG: Retractor, All Types

Sterilization

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

[07898506845392]

Moist Heat or Steam Sterilization

[07898506845392]

Moist Heat or Steam Sterilization

[07898506845392]

Moist Heat or Steam Sterilization

[07898506845392]

Moist Heat or Steam Sterilization

[07898506845392]

Moist Heat or Steam Sterilization

[07898506845392]

Moist Heat or Steam Sterilization

[07898506845392]

Moist Heat or Steam Sterilization

[07898506845392]

Moist Heat or Steam Sterilization

[07898506845392]

Moist Heat or Steam Sterilization

[07898506845392]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-11
• Device Publish Date: 2022-10-03

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