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Interlock™-35

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Interlock™-35 FDA UDI
Generic Name
Non-neurovascular embolization coil FDA UDI
Device Name
Fibered IDC™ Occlusion System FDA UDI
Model / Reference
M001363790 FDA UDI
Description
Fibered IDC™ Occlusion System FDA UDI

Identifiers

Catalog Number
M001363790 FDA UDI
Primary DI / UDI-DI
08714729793106 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

Yes

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: Non-neurovascular embolization coil

Interlock™-35 by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-neurovascular embolization coil.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI e79f7cde-8578-4a11-a600-54fde91a890d 35 fields · synced Jun 8, 2026