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Elevator

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
ELEVATOR FDA UDI
Generic Name
Dental elevator, tooth/root FDA UDI
Device Name
WINGED ELEVATOR #DELWING4 SHORT HANDLE FDA UDI
Model / Reference
1103-389C FDA UDI
Description
WINGED ELEVATOR #DELWING4 SHORT HANDLE FDA UDI

Identifiers

Catalog Number
1103-389C FDA UDI
Primary DI / UDI-DI
00192896052987 FDA UDI
FDA Product Code
EMJ FDA UDI
GMDN Term
Dental elevator, tooth/root 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

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

Dimensions & Sizes

Size
Length — 5.25 Inch FDA UDI

Category: Dental elevator, tooth/root

Elevator by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental elevator, tooth/root.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 73f48f32-53fc-42f4-aa6f-8a77acc0c830 36 fields · synced May 30, 2026