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Scanner, TxCell HS BM/BQ577

FDA UDI

Class II (US FDA UDI)

by Iridex Corporation

Identity

Trade Name
Scanner, TxCell HS BM/BQ577 FDA UDI
Generic Name
General/multiple surgical diode laser system FDA UDI
Model / Reference
70305 FDA UDI

Identifiers

Primary DI / UDI-DI
00813125016357 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
General/multiple surgical diode laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

Category: General/multiple surgical diode laser system

Scanner, TxCell HS BM/BQ577 by Iridex Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General/multiple surgical diode laser system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Iridex Corporation

Sources (1)

  • FDA UDI 613db8b8-19e3-448d-bde8-b6f724759089 33 fields · synced Jun 9, 2026