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GORE PRECLUDE Pericardial Membrane

FDA UDI

Class II (US FDA UDI)

by W. L. Gore & Associates, Inc

Identity

Trade Name
GORE PRECLUDE Pericardial Membrane FDA UDI
Generic Name
Pericardium prosthesis FDA UDI
Device Name
PRECLUDE PERICARDIAL MEMBRANE 12.0cmX12.0cmX0.1mm FDA UDI
Model / Reference
1PCM102 FDA UDI
Description
PRECLUDE PERICARDIAL MEMBRANE 12.0cmX12.0cmX0.1mm FDA UDI

Identifiers

Catalog Number
1PCM102 FDA UDI
Primary DI / UDI-DI
00733132601837 FDA UDI
510(k) Number
K012098 FDA UDI
FDA Product Code
DXZ FDA UDI
GMDN Term
Pericardium prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3470 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 12 Centimeter FDA UDI
Height — 0 Millimeter FDA UDI
Width — 12 Centimeter FDA UDI

Category: Pericardium prosthesis

GORE PRECLUDE Pericardial Membrane by W. L. Gore & Associates, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pericardium prosthesis.

Cleared under the same submission

K012098 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W. L. Gore & Associates, Inc

Sources (1)

  • FDA UDI ef2d9748-6c68-4400-8fab-f40363ecb8b8 37 fields · synced May 30, 2026