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Elevator #110 Bernard Left Dlc

FDA UDI

Class I (US FDA UDI)

by W.H. Holden, Inc.

Identity

Trade Name
ELEVATOR #110 BERNARD LEFT DLC FDA UDI
Generic Name
Dental elevator, tooth/root FDA UDI
Model / Reference
10-4110LDLC FDA UDI

Identifiers

Primary DI / UDI-DI
D928104110LDLC0 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental elevator, tooth/root

Elevator #110 Bernard Left Dlc by W.H. Holden, 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

Manufacturer
W.H. Holden, Inc.

Sources (1)

  • FDA UDI 9bc471e9-d07c-4715-8162-b48d167cb4b9 32 fields · synced Jun 1, 2026