Perchik Button™ H787138002015

GUDID 00884450786192

Merit Medical Systems, Inc.

Suture retention device

• Primary Device ID: 00884450786192
• NIH Device Record Key: 1b7e9b46-d0c6-46ef-a1eb-d6d4e726f1bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Perchik Button™
• Version Model Number: A
• Catalog Number: H787138002015
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 10
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450786192 [Unit of Use]
GS1	10884450786199 [Primary]

FDA Product Code

• KGS: RETENTION DEVICE, SUTURE

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-10
• Device Publish Date: 2024-07-02

Devices Manufactured by Merit Medical Systems, Inc.

• 10884450032364 - Merit Medical®: 2026-02-11
• 10884450121969 - Merit Medical®: 2026-02-11
• 10884450161392 - Merit Medical®: 2026-02-11
• 20884450436374 - Merit Medical®: 2026-02-11
• 10884450681203 - Preston™: 2026-02-11
• 00884450848135 - SerosaFuse®: 2026-02-11
• 20884450119604 - Prelude EASE™: 2026-02-11
• 20884450027183 - Merit Medical®: 2026-02-09