← Back to catalogue

GoldenDent

FDA UDI

Class I (US FDA UDI)

by GoldenDent

Identity

Trade Name
GoldenDent FDA UDI
Generic Name
Dappen dish, reusable FDA UDI
Device Name
Weighted Graft Material Dish FDA UDI
Model / Reference
GO WGD FDA UDI
Description
Weighted Graft Material Dish FDA UDI

Identifiers

Catalog Number
GO WGD FDA UDI
Primary DI / UDI-DI
00850011211922 FDA UDI
FDA Product Code
EKF FDA UDI
GMDN Term
Dappen dish, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dappen dish, reusable

GoldenDent by GoldenDent — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dappen dish, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
GoldenDent

Sources (1)

  • FDA UDI 1da71072-eb6c-42e7-a7c3-3f9d8ba2c986 34 fields · synced Jun 1, 2026