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Davis Mouth Gag Frame

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
DAVIS MOUTH GAG FRAME FDA UDI
Generic Name
Mouth gag, adjustable, reusable FDA UDI
Device Name
DAVIS MOUTH GAG BLADE WITHOUT ETHER TUBE SIZE 3 FDA UDI
Model / Reference
485-548 FDA UDI
Description
DAVIS MOUTH GAG BLADE WITHOUT ETHER TUBE SIZE 3 FDA UDI

Identifiers

Catalog Number
485-548 FDA UDI
Primary DI / UDI-DI
00192896043862 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Mouth gag, adjustable, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

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

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: Mouth gag, adjustable, reusable

Davis Mouth Gag Frame by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mouth gag, adjustable, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b13b2c5d-7967-46dd-8895-c085cf7ce46d 36 fields · synced Jun 8, 2026