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Upper DC Cable for v900L

FDA UDI

Class I (US FDA UDI)

by DermLite LLC

Identity

Trade Name
Upper DC Cable for v900L FDA UDI
Generic Name
Dermatoscope, optical FDA UDI
Device Name
Upper DC Cable for v900L FDA UDI
Model / Reference
Z1762-00 FDA UDI
Description
Upper DC Cable for v900L FDA UDI

Identifiers

Catalog Number
Z1762-00 FDA UDI
Primary DI / UDI-DI
00850017651326 FDA UDI
FDA Product Code
KYT FDA UDI
GMDN Term
Dermatoscope, optical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6350 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dermatoscope, optical

Upper DC Cable for v900L by DermLite LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatoscope, optical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DermLite LLC

Sources (1)

  • FDA UDI ba55e453-5f59-4cdd-878c-6d6ff7f24230 35 fields · synced May 30, 2026