STERIL-PEEL

GUDID D8302214341

STERIL-PEEL TUBING/ROLL 4" X 100'

GS Medical Packaging Inc

Sterilization packaging, single-use

• Primary Device ID: D8302214341
• NIH Device Record Key: 2bb20e38-8bed-4cc5-a2e1-473fc688a1a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STERIL-PEEL
• Version Model Number: 221434
• 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

Customer Support Contacts

• Phone: 9052711523
• Email: accounting@gsmedicalpackaging.com
• Phone: 9052711523
• Email: accounting@gsmedicalpackaging.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D830221434 [Primary]
HIBCC	D8302214340 [Package]; Contains: D830221434; Package: POLY BAG [1 Units]; In Commercial Distribution
HIBCC	D8302214341 [Package]; Contains: D8302214340; Package: CARDBOARD BOX [10 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: 2016-10-05

On-Brand Devices [STERIL-PEEL]

• D8302228162: STERIL-PEEL SS POUCH 8" X 16"
• D8302225552: STERIL-PEEL SS POUCH 12" X 15"
• D830222103B2: UNPRINTED SS POUCH 7.5" X 13"
• D8302214341: STERIL-PEEL TUBING/ROLL 4" X 100'