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X-Seed

FDA UDI

Class II (US FDA UDI)

by Izi Medical Products Llc

Identity

Trade Name
X-Seed FDA UDI
Generic Name
Radiological image marker, implantable FDA UDI
Device Name
1.15mm x 5mm X-SEED Single Pack FDA UDI
Model / Reference
215001 FDA UDI
Description
1.15mm x 5mm X-SEED Single Pack FDA UDI

Identifiers

Catalog Number
215001 FDA UDI
Primary DI / UDI-DI
EIBA2150010 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Radiological image marker, implantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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

Category: Radiological image marker, implantable

X-Seed by Izi Medical Products Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological image marker, implantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 85518f94-7935-479a-9312-7c86e292924d 36 fields · synced May 30, 2026