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RUBY Coil

FDA UDI

Class II (US FDA UDI)

by Penumbra, Inc.

Identity

Trade Name
RUBY Coil FDA UDI
Generic Name
Embolization implant kit FDA UDI
Device Name
Ruby Standard, 28x60 FDA UDI
Model / Reference
RBY2C2860-B FDA UDI
Description
Ruby Standard, 28x60 FDA UDI

Identifiers

Catalog Number
RBY2C2860 FDA UDI
Primary DI / UDI-DI
00814548019314 FDA UDI
510(k) Number
K173614 FDA UDI
FDA Product Code
KRD FDA UDI
GMDN Term
Embolization implant kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Embolization implant kit

RUBY Coil by Penumbra, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Embolization implant kit.

Cleared under the same submission

K173614 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Penumbra, Inc.

Sources (1)

  • FDA UDI c68fe61a-7fdb-4334-94ac-430572f3edea 35 fields · synced May 31, 2026