Identity
- Trade Name
- RUBY FDA UDI
- Generic Name
- Non-neurovascular embolization coil FDA UDI
- Device Name
- Ruby Standard, 20mm x 60cm FDA UDI
- Model / Reference
- RBY2C2060-B FDA UDI
- Description
- Ruby Standard, 20mm x 60cm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00814548019284 FDA UDI
- 510(k) Number
- K173614 FDA UDI
- FDA Product Code
- KRD FDA UDIHCG FDA UDI
- GMDN Term
- Non-neurovascular embolization coil FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.3300 FDA UDI882.5950 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
MR Conditional FDA UDI
Category: Non-neurovascular embolization coil
Ruby by Penumbra, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Non-neurovascular embolization coil.
- ConcertoTM — Micro Therapeutics, Inc. · Class II
- Target — Stryker Corp. · Class II
- Prestige Coil System — BALT USA LLC · Class II
- Optima Coil System — BALT USA LLC · Class II
- Nester — COOK INCORPORATED · Class II
- ConcertoTM — Micro Therapeutics, Inc. · Class II
- TARGET — Stryker Corp. · Class II
- GDC-10 — Stryker Corp. · Class II
Cleared under the same submission
K173614 also covers:
- POD — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
- Penumbra Coil 400 — PENUMBRA, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Penumbra, Inc.
Sources (1)
- FDA UDI dd8537fc-43fe-4e07-a5aa-9429eb432ef0 34 fields · synced Jun 6, 2026