AHLGeneric

GUDID 05056009101236

Temporary Cavity Filling Material

ADVANCED HEALTHCARE LTD.

Gynaecological biopsy forceps, reusable

• Primary Device ID: 05056009101236
• NIH Device Record Key: dfdfec90-fdf5-4cc9-afe5-dcff906bbbe5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AHLGeneric
• Version Model Number: 009X7
• Company DUNS: 298822065
• Company Name: ADVANCED HEALTHCARE LTD.
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +441892870500
• Email: sales@ahl.uk.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05056009101236 [Primary]

FDA Product Code

• EMA: Cement, Dental

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: 2018-03-29
• Device Publish Date: 2016-09-06

On-Brand Devices [AHLGeneric]

• 05056009101243: Temporary Filling Material 30g (NEW JAR)
• 05056009101236: Temporary Cavity Filling Material