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Dmv 45

FDA UDI

Class I (US FDA UDI)

by DMV Corporation

Identity

Trade Name
DMV 45 FDA UDI
Generic Name
Rigid contact lens inserter/remover FDA UDI
Device Name
CL remover/inserter for hard and gp CL with 45° tilted suction cup FDA UDI
Model / Reference
585 FDA UDI
Description
CL remover/inserter for hard and gp CL with 45° tilted suction cup FDA UDI

Identifiers

Catalog Number
585 FDA UDI
Primary DI / UDI-DI
00080875975856 FDA UDI
510(k) Number
K830496 FDA UDI
FDA Product Code
KYE FDA UDI
GMDN Term
Rigid contact lens inserter/remover FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5420 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rigid contact lens inserter/remover

Dmv 45 by DMV Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid contact lens inserter/remover.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DMV Corporation

Sources (1)

  • FDA UDI dc66f217-8915-4bb5-9bf2-2561ad65627d 35 fields · synced Jun 8, 2026