Sani-Spec

GUDID 40888937010143

Sani-Spec® Disposable Specula • Medium

Coopersurgical, Inc.

Vaginal speculum, single-use

• Primary Device ID: 40888937010143
• NIH Device Record Key: 46baacee-28fd-48df-ba62-253e3cdfa43d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sani-Spec
• Version Model Number: 82330
• Company DUNS: 801895244
• Company Name: Coopersurgical, Inc.
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	20888937010149 [Package]; Contains: 50888937010140; Package: [10 Units]; In Commercial Distribution
GS1	30888937010146 [Package]; Contains: 20888937010149; Package: [4 Units]; In Commercial Distribution
GS1	40888937010143 [Package]; Contains: 30888937010146; Package: [48 Units]; In Commercial Distribution
GS1	50888937010140 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K841909

FDA Product Code

• HIB: Speculum, Vaginal, Nonmetal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

On-Brand Devices [Sani-Spec]

• 20888937010156: Sani-Spec® Disposable Specula • Large
• 40888937010143: Sani-Spec® Disposable Specula • Medium
• 40888937010136: Sani-Spec® Disposable Specula • Small
• 40888937012451: Sani-Spec® Disposable Speculum 1 Vaginal Speculum • Medium
• 40888937012444: Sani-Spec® Disposable Speculum 1 Vaginal Speculum • Small