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Amplatzer™

FDA UDI

Class II (US FDA UDI)

by Aga Medical Corp.

Identity

Trade Name
AMPLATZER™ FDA UDI
Generic Name
Non-neurovascular embolization plug, metallic FDA UDI
Device Name
Vascular Plug FDA UDI
Model / Reference
9-PLUG-008 FDA UDI
Description
Vascular Plug FDA UDI

Identifiers

Catalog Number
9-PLUG-008 FDA UDI
Primary DI / UDI-DI
00811806011462 FDA UDI
FDA Product Code
KRD FDA UDI
GMDN Term
Non-neurovascular embolization plug, metallic 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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 8 Millimeter FDA UDI

Category: Non-neurovascular embolization plug, metallic

Amplatzer™ by Aga Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-neurovascular embolization plug, metallic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aga Medical Corp.

Sources (1)

  • FDA UDI d8669353-0e1a-4a42-b522-477451eb6c7c 37 fields · synced May 30, 2026