VWR

GUDID D830VWR891408022

VWR S/S 7.5"X13"(1000)

GS Medical Packaging Inc

Sterilization packaging, single-use

• Primary Device ID: D830VWR891408022
• NIH Device Record Key: 568a8a77-6da7-4a97-a8a3-12d59a5a8384
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VWR
• Version Model Number: VWR89140802
• Company DUNS: 246113039
• Company Name: GS Medical Packaging 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: 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
HIBCC	D830VWR89140802 [Primary]
HIBCC	D830VWR891408021 [Package]; Contains: D830VWR89140802; Package: CARDBOARD BOX [200 Units]; In Commercial Distribution
HIBCC	D830VWR891408022 [Package]; Contains: D830VWR891408021; Package: CARDBOARD BOX [1000 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K953829

FDA Product Code

• KCT: Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-08
• Device Publish Date: 2017-02-07

On-Brand Devices [VWR]

• D830VWR891408042: VWR S/S 12"X18" (400)
• D830VWR891408022: VWR S/S 7.5"X13"(1000)
• D830VWR891408002: VWR S/S 5.25"x10" (1200)