← Back to catalogue

A. Titan Instruments

FDA UDI

Class I (US FDA UDI)

by A.Titan Instruments

Identity

Trade Name
A. Titan Instruments FDA UDI
Generic Name
Mouth gag, non-adjustable FDA UDI
Device Name
Mouth Prop, for Adults FDA UDI
Model / Reference
1115-14 FDA UDI
Description
Mouth Prop, for Adults FDA UDI

Identifiers

Primary DI / UDI-DI
00841685102456 FDA UDI
FDA Product Code
EIG FDA UDI
GMDN Term
Mouth gag, non-adjustable 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

No

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Category: Mouth gag, non-adjustable

A. Titan Instruments by A.Titan Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mouth gag, non-adjustable.

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
A.Titan Instruments

Sources (1)

  • FDA UDI ba3d830e-34f4-4f1a-b1f7-4a070f962385 33 fields · synced Jun 9, 2026