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Hmr-272a

FDA UDI

Class II (US FDA UDI)

by International Medical Lasers, Inc.

Identity

Trade Name
HMR-272A FDA UDI
Generic Name
General/multiple surgical laser system beam guide, reusable FDA UDI
Device Name
Reusable Surgical Laser Fiber 272/300/450, hard clad, blue tefzel, NA 0.22, Absorbing Dark Hole Connector® SMA905 , reusable, blue extension sleeves with logo, EO sterile, Flat Tip, IML label FDA UDI
Model / Reference
HMR-272A FDA UDI
Description
Reusable Surgical Laser Fiber 272/300/450, hard clad, blue tefzel, NA 0.22, Absorbing Dark Hole Connector® SMA905 , reusable, blue extension sleeves with logo, EO sterile, Flat Tip, IML label FDA UDI

Identifiers

Primary DI / UDI-DI
00851272007156 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

Yes

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

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

Hmr-272a by International Medical Lasers, 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a8f91ab3-4f13-40e7-ba57-d7eb86dbbc74 34 fields · synced May 30, 2026