← Back to catalogue

Promark Touch Probe

FDA UDI

Class U (US FDA UDI)

by VDW GmbH

Identity

Trade Name
PROMARK TOUCH PROBE FDA UDI
Generic Name
Endodontic apex locator FDA UDI
Model / Reference
V841119000518 FDA UDI

Identifiers

Catalog Number
V841119000518 FDA UDI
Primary DI / UDI-DI
E225V8411190005181 FDA UDI
FDA Product Code
LQY FDA UDI
GMDN Term
Endodontic apex locator FDA UDI

Classification

Device Class
U 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
Moist Heat or Steam Sterilization FDA UDI

Category: Endodontic apex locator

Promark Touch Probe by VDW GmbH — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic apex locator.

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
VDW GmbH

Sources (1)

  • FDA UDI dbd623ec-57ee-48ef-83e5-846105ba4335 33 fields · synced Jun 8, 2026