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Gps

FDA UDI

Class I (US FDA UDI)

by Group Practice Solutions

Identity

Trade Name
GPS FDA UDI
Generic Name
Digital imaging cassette/storage phosphor screen, dental FDA UDI
Device Name
BARRIER ENVELOPES SIZE 0 FDA UDI
Model / Reference
45-8700 FDA UDI
Description
BARRIER ENVELOPES SIZE 0 FDA UDI

Identifiers

Primary DI / UDI-DI
00817800020479 FDA UDI
FDA Product Code
IXC FDA UDI
GMDN Term
Digital imaging cassette/storage phosphor screen, dental FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1890 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Digital imaging cassette/storage phosphor screen, dental

Gps by Group Practice Solutions — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Digital imaging cassette/storage phosphor screen, dental.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Group Practice Solutions

Sources (1)

  • FDA UDI aeb13f01-1fe1-4082-a0f3-c8e7e7cd9af0 33 fields · synced May 30, 2026