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Connected OR HUB

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Connected OR HUB FDA UDI
Generic Name
Endoscopic device remote control FDA UDI
Model / Reference
0240200102 FDA UDI

Identifiers

Catalog Number
0240200102 FDA UDI
Primary DI / UDI-DI
07613327419146 FDA UDI
510(k) Number
K181258 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscopic device remote control 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

Category: Endoscopic device remote control

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

Similar devices

Also classified as Endoscopic device remote control.

Cleared under the same submission

K181258 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 9da3e952-90c6-4b00-a76b-4a41dfd79681 35 fields · synced May 30, 2026