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25GA Curved Laser Probe - Iridex

FDA UDI

Class II (US FDA UDI)

by Peregrine Surgical, LLC.

Identity

Trade Name
25GA Curved Laser Probe - Iridex FDA UDI
Generic Name
Ophthalmic laser system beam guide FDA UDI
Device Name
25GA Curved Laser Probe - Iridex FDA UDI
Model / Reference
PD725.22 FDA UDI
Description
25GA Curved Laser Probe - Iridex FDA UDI

Identifiers

Primary DI / UDI-DI
00632307000720 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 — 25 Gauge FDA UDI

Category: Ophthalmic laser system beam guide

25GA Curved Laser Probe - Iridex 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

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Manufacturer

Sources (1)

  • FDA UDI 531818f4-7507-430f-bc37-4c230b8479df 36 fields · synced Jun 8, 2026