← Back to catalogue

20GA Straight Laser Probe - HGM

FDA UDI

Class II (US FDA UDI)

by Peregrine Surgical, LLC.

Identity

Trade Name
20GA Straight Laser Probe - HGM FDA UDI
Generic Name
Ophthalmic laser system beam guide FDA UDI
Device Name
20GA Straight Laser Probe - HGM FDA UDI
Model / Reference
PD720.11 FDA UDI
Description
20GA Straight Laser Probe - HGM FDA UDI

Identifiers

Primary DI / UDI-DI
00632307000133 FDA UDI
510(k) Number
K024061 FDA UDI
FDA Product Code
HQF FDA UDI
GEX FDA UDI
GMDN Term
Ophthalmic laser system beam guide FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4390 FDA UDI
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
Needle Gauge — 20 Gauge FDA UDI

Category: Ophthalmic laser system beam guide

20GA Straight Laser Probe - HGM by Peregrine Surgical, LLC. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic laser system beam guide.

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 33fcc6d0-b0c1-48b9-8726-22db64f80cb0 36 fields · synced May 30, 2026