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1788

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
1788 FDA UDI
Generic Name
Endoscope video camera FDA UDI
Device Name
1788 4K Inline Camera Head, C-Mount FDA UDI
Model / Reference
1788710105 FDA UDI
Description
1788 4K Inline Camera Head, C-Mount FDA UDI

Identifiers

Catalog Number
1788710105 FDA UDI
Primary DI / UDI-DI
07613327580082 FDA UDI
510(k) Number
K230605 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscope video camera 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

No

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
Sterilization Method
Hydrogen Peroxide FDA UDI

Category: Endoscope video camera

1788 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope video camera.

Cleared under the same submission

K230605 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 7fb1612a-aec5-4e64-ab9d-cde725689494 36 fields · synced Jun 8, 2026