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Sunoptic Technologies

FDA UDI

Class I (US FDA UDI)

by Sunoptic Technologies

Identity

Trade Name
Sunoptic Technologies FDA UDI
Generic Name
Surgical video camera FDA UDI
Device Name
camera systems FDA UDI
Model / Reference
Camera System FDA UDI
Description
camera systems FDA UDI

Identifiers

Primary DI / UDI-DI
M678CS0 FDA UDI
FDA Product Code
FWF FDA UDI
KQM FDA UDI
GMDN Term
Surgical video camera FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical video camera

Sunoptic Technologies by Sunoptic Technologies — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical video camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 79555a67-ddac-4c64-ade7-7f64fc2b9738 34 fields · synced May 29, 2026