← Back to catalogue

Ideal Eyes

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Ideal Eyes FDA UDI
Generic Name
Flexible-tip video laparoscope FDA UDI
Device Name
HD Articulating Laparoscope FDA UDI
Model / Reference
0502110110 FDA UDI
Description
HD Articulating Laparoscope FDA UDI

Identifiers

Catalog Number
0502-110-110 FDA UDI
Primary DI / UDI-DI
07613327062243 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Flexible-tip video laparoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 5.0 Millimeter FDA UDI

Category: Flexible-tip video laparoscope

Ideal Eyes by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible-tip video laparoscope.

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
Stryker Corp.

Sources (1)

  • FDA UDI e0d30af2-175e-4a0b-b65e-5a47a6b23d00 36 fields · synced May 30, 2026