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Wrapsody®

FDA UDI

Class III (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
WRAPSODY® FDA UDI
Generic Name
Central/peripheral venous endovascular stent-graft FDA UDI
Model / Reference
A FDA UDI

Identifiers

Catalog Number
WRAP-L16030 FDA UDI
Primary DI / UDI-DI
00884450845738 FDA UDI
FDA Product Code
PFV FDA UDI
GMDN Term
Central/peripheral venous endovascular stent-graft FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Central/peripheral venous endovascular stent-graft

Wrapsody® by Merit Medical Systems, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Central/peripheral venous endovascular stent-graft.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI 08777580-5688-4149-ab38-4fcb9bf71f8b 34 fields · synced Jun 9, 2026