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Misago®

FDA UDI

Class III (US FDA UDI)

by Terumo Corp.

Identity

Trade Name
Misago® FDA UDI
Generic Name
Peripheral artery stent, bare-metal FDA UDI
Device Name
MISAGO RX Self-expanding Peripheral Stent FDA UDI
Model / Reference
SXR08080L FDA UDI
Description
MISAGO RX Self-expanding Peripheral Stent FDA UDI

Identifiers

Catalog Number
SX*FXA0880LN FDA UDI
Primary DI / UDI-DI
04987350722324 FDA UDI
FDA Product Code
NIP FDA UDI
GMDN Term
Peripheral artery stent, bare-metal 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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 80 Millimeter FDA UDI
Lumen/Inner Diameter — 8 Millimeter FDA UDI

Category: Peripheral artery stent, bare-metal

Misago® by Terumo Corp. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral artery stent, bare-metal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terumo Corp.

Sources (1)

  • FDA UDI fcfc8483-721c-4024-b544-dfacd59b8450 37 fields · synced May 31, 2026