ASAPLP™ ASAPLP/B

GUDID 10884450160579

Merit Medical Systems, Inc.

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Primary Device ID	10884450160579
NIH Device Record Key	937e22d8-2716-4e87-928d-128df885ca0f
Commercial Distribution Status	In Commercial Distribution
Brand Name	ASAPLP™
Version Model Number	00884450160572
Catalog Number	ASAPLP/B
Company DUNS	184763290
Company Name	Merit Medical Systems, 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	false
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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450160572 [Primary]
GS1	10884450160579 [Package] Contains: 00884450160572 Package: [3 Units] In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K132155

FDA Product Code

DXE	Catheter, embolectomy

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	3
Public Version Date	2018-07-06
Device Publish Date	2016-12-05

On-Brand Devices [ASAPLP™]

10884450329303	00884450329306
10884450160579	00884450160572
10884450511746	00884450511749
10884450555122	00884450555125