Procam HD II RX2

Procam HD II RX2 (U1VI3603) is a Class I device made by Ecleris, listed in FDA GUDID since 30 Jul 2025 (UDI-DI B366U1VI3603RX2), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberB366U1VI3603RX2 UDI-DI	Date30 Jul 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Procam HD II
Generic name: Surgical video camera
Model / Ref / Catalog: RX2, U1VI3603

Primary DI / UDI-DI: B366U1VI3603RX2
FDA product code: FWD
GMDN term: Surgical video camera

Device class: Class I
Regulation number: 878.4160
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Surgical video camera.

Other devices from Ecleris

Portaled R00

Class I
Portaled RX1

Class I
Procam 4K R00

Class I
Procam 4K USB RX1

Class I

See all devices from Ecleris →

Properties

Premarket exempt
Serial number
Manufacturing date

Other properties (12, all answered No)