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Dmg

FDA UDI

Class II (US FDA UDI)

by DMG America LLC

Identity

Trade Name
DMG FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
DMG StatusBlue (8) cartridges 50ml FDA UDI
Model / Reference
999826 FDA UDI
Description
DMG StatusBlue (8) cartridges 50ml FDA UDI

Identifiers

Catalog Number
999826 FDA UDI
Primary DI / UDI-DI
D0339998261 FDA UDI
510(k) Number
K013237 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Dimensions & Sizes

Size
Total Volume — 50 Milliliter FDA UDI

Category: Dental composite resin

Dmg by DMG America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DMG America LLC

Sources (1)

  • FDA UDI 61e91070-706a-45f2-b1bb-2ea9ea05fc0a 38 fields · synced Jun 8, 2026