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Dental City

FDA UDI

Class II (US FDA UDI)

by Icp, Inc.

Identity

Trade Name
Dental City FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
Dental City Sterilization Pouches 2.25x4 200/Box FDA UDI
Model / Reference
60-429 FDA UDI
Description
Dental City Sterilization Pouches 2.25x4 200/Box FDA UDI

Identifiers

Primary DI / UDI-DI
D77160429 FDA UDI
FDA Product Code
JOJ FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 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

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

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: Sterilization packaging, single-use

Dental City by Icp, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization packaging, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icp, Inc.

Sources (1)

  • FDA UDI f2772665-f9dd-4580-ab85-a6259c2266bc 33 fields · synced May 30, 2026