DENALI

GUDID 00810042120273

Curved Bracket Tweezer

ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC

Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable Dressing/utility forceps, tweezers-like, reusable

• Primary Device ID: 00810042120273
• NIH Device Record Key: 26923203-5f4a-477f-826c-a23a54412d9b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DENALI
• Version Model Number: 0112-204
• Company DUNS: 077801124
• Company Name: ORTHODONTIC SUPPLY & EQUIPMENT COMPANY 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810042120273 [Primary]

FDA Product Code

• KCX: Epilator, High Frequency, Tweezer-Type

Sterilization

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

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

[00810042120273]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-07-23
• Device Publish Date: 2020-04-21

On-Brand Devices [DENALI]

• 00810042120273: Curved Bracket Tweezer
• 00810042120266: Reverse Action Keat Buccal Tube Tweezer
• 00810042120259: Keat Buccal Tube Tweezer
• 00810042120242: Bracket Tweezer - Standard Large
• 00810042120235: Bracket Tweezer - Standard Small