ReSolve CirQ™ RCQH-10-038MB

GUDID 00884450400173

Merit Medical Systems, Inc.

Closed-wound drain Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable

Primary Device ID	00884450400173
NIH Device Record Key	53794689-7209-454b-9833-f7cc8fbac4e2
Commercial Distribution Status	In Commercial Distribution
Brand Name	ReSolve CirQ™
Version Model Number	00884450400173
Catalog Number	RCQH-10-038MB
Company DUNS	184763290
Company Name	Merit Medical Systems, Inc.
Device Count	1
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	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	00884450400173 [Primary]

FDA Product Code

GBO	CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY

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	2019-02-15
Device Publish Date	2019-01-15

On-Brand Devices [ReSolve CirQ™]

00884450400173	00884450400173
00884450358900	00884450358900