Forceps - Adson type Forceps - Adson type

GUDID 00083208190148

Adson Tissue Forceps are used for holding and manipulating delicate tissues.

Suncoast Dental, Inc

Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable

• Primary Device ID: 00083208190148
• NIH Device Record Key: 0c0fc4be-a773-4c59-8d1b-e023053b3f9f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Forceps - Adson type
• Version Model Number: Forceps - Adson type
• Catalog Number: Forceps - Adson type
• Company DUNS: 078352849
• Company Name: Suncoast Dental, Inc
• 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

Customer Support Contacts

• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com
• Phone: 727-536-4880
• Email: tatumcompliance@gmail.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00083208190148 [Primary]

FDA Product Code

• DZN: Instruments, Dental Hand

Sterilization

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

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

[00083208190148]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-11
• Device Publish Date: 2021-02-03

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