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Bead Block™

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Bead Block™ FDA UDI
Generic Name
Embolization particle, non-bioabsorbable FDA UDI
Device Name
Bland Embolic Bead FDA UDI
Model / Reference
EB2S305-US FDA UDI
Description
Bland Embolic Bead FDA UDI

Identifiers

Catalog Number
EB2S305-US FDA UDI
Primary DI / UDI-DI
00191506011352 FDA UDI
FDA Product Code
KRD FDA UDI
NOY FDA UDI
NAJ FDA UDI
HCG FDA UDI
GMDN Term
Embolization particle, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3300 FDA UDI
876.5550 FDA UDI
882.5950 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
MRI Safety
MR Safe FDA UDI

Category: Embolization particle, non-bioabsorbable

Bead Block™ by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Embolization particle, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 769c5836-8fd4-4dcf-b58d-c91f67eb3ccb 34 fields · synced Jun 8, 2026