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Hilal

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Hilal FDA UDI
Generic Name
Non-neurovascular embolization coil FDA UDI
Device Name
Hilal Embolization Microcoil FDA UDI
Model / Reference
G47498 FDA UDI
Description
Hilal Embolization Microcoil FDA UDI

Identifiers

Catalog Number
MWCE-18-0.5-0-HILAL-01 FDA UDI
Primary DI / UDI-DI
00827002474987 FDA UDI
510(k) Number
K160219 FDA UDI
FDA Product Code
KRD FDA UDI
GMDN Term
Non-neurovascular embolization coil 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

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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Non-neurovascular embolization coil

Hilal by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-neurovascular embolization coil.

Cleared under the same submission

K160219 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 4284268c-9152-4882-b4ff-cf3a307c1a68 37 fields · synced Jun 6, 2026