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Dgc-30-5

FDA UDI

Class I (US FDA UDI)

by Izi Medical Products Llc

Identity

Trade Name
DGC-30-5 FDA UDI
Generic Name
Imaging lesion localization marker, external, single-use FDA UDI
Model / Reference
G04303 FDA UDI

Identifiers

Primary DI / UDI-DI
00815212024306 FDA UDI
FDA Product Code
MIJ FDA UDI
GMDN Term
Imaging lesion localization marker, external, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Imaging lesion localization marker, external, single-use

Dgc-30-5 by Izi Medical Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Imaging lesion localization marker, external, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8cd2edc6-32ab-46c9-9fab-6bb38b30935b 32 fields · synced May 31, 2026