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VereSee

FDA UDI

Class II (US FDA UDI)

by Freyja Healthcare, Llc

Identity

Trade Name
VereSee FDA UDI
Generic Name
Camera control unit FDA UDI
Device Name
VereSee, Camera Control Unit FDA UDI
Model / Reference
VER-100-103 FDA UDI
Description
VereSee, Camera Control Unit FDA UDI

Identifiers

Primary DI / UDI-DI
00860012249954 FDA UDI
510(k) Number
K232464 FDA UDI
FDA Product Code
HIF FDA UDI
GMDN Term
Camera control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1730 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 3 Pound FDA UDI

Category: Camera control unit

VereSee by Freyja Healthcare, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Camera control unit.

Cleared under the same submission

K232464 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Freyja Healthcare, Llc

Sources (1)

  • FDA UDI dbd14cc8-dabb-4fad-8d73-e0eaaf1c121b 36 fields · synced May 30, 2026