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HydroPearl

FDA UDI

Class II (US FDA UDI)

by Microvention Inc.

Identity

Trade Name
HydroPearl FDA UDI
Generic Name
Embolization particle, non-bioabsorbable FDA UDI
Device Name
Bland Beads FDA UDI
Model / Reference
HP2S0400 FDA UDI
Description
Bland Beads FDA UDI

Identifiers

Catalog Number
HP2S0400 FDA UDI
Primary DI / UDI-DI
00816777026101 FDA UDI
510(k) Number
K150870 FDA UDI
FDA Product Code
NAJ FDA UDI
GMDN Term
Embolization particle, non-bioabsorbable 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 Safe FDA UDI

Category: Embolization particle, non-bioabsorbable

HydroPearl by Microvention Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Embolization particle, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microvention Inc.

Sources (1)

  • FDA UDI c713d791-5786-4cd5-b7f4-5cfbb4add3c3 37 fields · synced Jun 8, 2026