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Collagentex Series

FDA UDI

Class II (US FDA UDI)

by Tanses Technologies Inc

Identity

Trade Name
Collagentex Series FDA UDI
Generic Name
Red-light phototherapy unit, professional FDA UDI
Device Name
Collagentex Rx-1-Seat NIR device, Seat version, model Rx-1-Seat, 1 lamp module FDA UDI
Model / Reference
RX-1-Seat FDA UDI
Description
Collagentex Rx-1-Seat NIR device, Seat version, model Rx-1-Seat, 1 lamp module FDA UDI

Identifiers

Primary DI / UDI-DI
00850056256414 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Red-light phototherapy unit, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 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

Yes

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: Red-light phototherapy unit, professional

Collagentex Series by Tanses Technologies Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Red-light phototherapy unit, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0ef5500e-4298-4fe8-a044-d460d7f118ba 34 fields · synced May 30, 2026