← Back to catalogue

Wingman

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Wingman FDA UDI
Generic Name
Surgical camera holder FDA UDI
Device Name
Scope Holder FDA UDI
Model / Reference
0240240000 FDA UDI
Description
Scope Holder FDA UDI

Identifiers

Catalog Number
0240-240-000 FDA UDI
Primary DI / UDI-DI
07613327056259 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Surgical camera holder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

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: Surgical camera holder

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

Similar devices

Also classified as Surgical camera holder.

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 55e56ba9-d680-4fe9-8b1a-7740ef3d0879 35 fields · synced May 30, 2026