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Connect OR OS

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Connect OR OS FDA UDI
Generic Name
Operating room audiovisual data/device management system application software FDA UDI
Model / Reference
0240060140 FDA UDI

Identifiers

Catalog Number
0240-060-140 FDA UDI
Primary DI / UDI-DI
07613327311839 FDA UDI
510(k) Number
K160332 FDA UDI
FDA Product Code
HRX FDA UDI
GCJ FDA UDI
GMDN Term
Operating room audiovisual data/device management system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
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: Operating room audiovisual data/device management system application software

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

Similar devices

Also classified as Operating room audiovisual data/device management system application software.

Cleared under the same submission

K160332 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 e290a20f-d314-4a8f-9877-296bd0e70b2b 35 fields · synced Jun 8, 2026