← Back to catalogue

Steri-Shield

FDA UDI

Class I (US FDA UDI)

by Steri-Shield Products, Inc.

Identity

Trade Name
Steri-Shield FDA UDI
Generic Name
Dental x-ray film holder, single-use FDA UDI
Device Name
Wingers-P, LG Case FDA UDI
Model / Reference
088-034 FDA UDI
Description
Wingers-P, LG Case FDA UDI

Identifiers

Primary DI / UDI-DI
10850040097129 FDA UDI
FDA Product Code
EGZ FDA UDI
GMDN Term
Dental x-ray film holder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.1905 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

No

FDA UDI

Category: Dental x-ray film holder, single-use

Steri-Shield by Steri-Shield Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental x-ray film holder, single-use.

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
Steri-Shield Products, Inc.

Sources (1)

  • FDA UDI 9a94ec4d-d4bb-4c29-9889-daebfd87b453 33 fields · synced May 30, 2026