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Trimedyne® FlexMax® 200 µm Reusable Fiber (SMA Connector), 5m Length

FDA UDI

Class II (US FDA UDI)

by Trimedyne, Inc.

Identity

Trade Name
Trimedyne® FlexMax® 200 µm Reusable Fiber (SMA Connector), 5m Length FDA UDI
Generic Name
General/multiple surgical laser system beam guide, reusable FDA UDI
Device Name
Fiber, Bare, 200um, Reusable, SMA Connector, 5m long FDA UDI
Model / Reference
B2005M-SMA FDA UDI
Description
Fiber, Bare, 200um, Reusable, SMA Connector, 5m long FDA UDI

Identifiers

Catalog Number
B2005M-SMA FDA UDI
Primary DI / UDI-DI
M473B2005MSMA0 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
General/multiple surgical laser system beam guide, reusable 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General/multiple surgical laser system beam guide, reusable

Trimedyne® FlexMax® 200 µm Reusable Fiber (SMA Connector), 5m Length by Trimedyne, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as General/multiple surgical laser system beam guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trimedyne, Inc.

Sources (1)

  • FDA UDI 556891d8-6552-42d3-b326-eb95ed3b3a5e 35 fields · synced May 30, 2026