DV-53 CHILD TWIN PEDO PAK

GUDID 00812045030948

D Speed, Size 0, 100 Double Film Packets.

Flow X Ray Corporation

Dental x-ray film, non-screen

• Primary Device ID: 00812045030948
• NIH Device Record Key: a313535f-6f74-4481-a0a1-d23d5efcb1f6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DV-53 CHILD TWIN PEDO PAK
• Version Model Number: 18236
• Company DUNS: 010016319
• Company Name: Flow X Ray Corporation
• Device Count: 100
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	00812045030948 [Primary]
GS1	10812045030945 [Package]; Package: [50 Units]; In Commercial Distribution
GS1	20812045030942 [Unit of Use]

FDA Product Code

• IWZ: Film, Radiographic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-17
• Device Publish Date: 2023-08-09

On-Brand Devices [DV-53 CHILD TWIN PEDO PAK]

• 00812045030948: D Speed, Size 0, 100 Double Film Packets.
• 00812045030849: D Speed, Size 0, 100 Double Film Packets.