← Back to catalogue

ScopeSafe™Laser Fiber

FDA UDI

Class II (US FDA UDI)

by Optical Integrity, Inc.

Identity

Trade Name
ScopeSafe™Laser Fiber FDA UDI
Generic Name
General/multiple surgical laser system beam guide, reusable FDA UDI
Device Name
200 micrometer ScopeSafe laser fiber, Trimedyne compatible FDA UDI
Model / Reference
10840 FDA UDI
Description
200 micrometer ScopeSafe laser fiber, Trimedyne compatible FDA UDI

Identifiers

Primary DI / UDI-DI
B145108400 FDA UDI
510(k) Number
K022338 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

Yes

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 200 Micrometer FDA UDI

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

Get a safe and reliable laser fiber for your general, multiple surgical laser system beam guide. Optical Integrity Inc's ScopeSafe Laser Fiber is a reusable device designed for versatile use in various surgical applications.

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3d75d075-4caf-4a18-bb4b-0ad012847061 37 fields · synced Jun 24, 2026