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Adler MicroMed Laser Surgery Fiber

FDA UDI

Class II (US FDA UDI)

by Adler MicroMed, Inc.

Identity

Trade Name
Adler MicroMed Laser Surgery Fiber FDA UDI
Generic Name
General/multiple surgical laser system beam guide, reusable FDA UDI
Device Name
Adler MicroMed Laser Surgery Fiber 3.0 NC 270 HGT 420 RT FDA UDI
Model / Reference
BFCS000296 FDA UDI
Description
Adler MicroMed Laser Surgery Fiber 3.0 NC 270 HGT 420 RT FDA UDI

Identifiers

Catalog Number
BFCS000296 FDA UDI
Primary DI / UDI-DI
00850348007212 FDA UDI
510(k) Number
K152417 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

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

Adler MicroMed Laser Surgery Fiber by Adler MicroMed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

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Manufacturer

Sources (1)

  • FDA UDI 59af78e3-c4f7-449d-bd42-d70bd152bffb 35 fields · synced May 30, 2026