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Lasercyn Dermal Spray

FDA UDI

Class U (US FDA UDI)

by Sonoma Pharmaceuticals, Inc.

Identity

Trade Name
Lasercyn Dermal Spray FDA UDI
Generic Name
Non-antimicrobial wound irrigation solution, multiple solute FDA UDI
Model / Reference
84993 FDA UDI

Identifiers

Catalog Number
84993 FDA UDI
Primary DI / UDI-DI
00867784000189 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Non-antimicrobial wound irrigation solution, multiple solute FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 59 Milliliter FDA UDI

Category: Non-antimicrobial wound irrigation solution, multiple solute

Lasercyn Dermal Spray by Sonoma Pharmaceuticals, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-antimicrobial wound irrigation solution, multiple solute.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fd16a24d-2a45-4a68-b41d-26a46e87c7f4 35 fields · synced Jun 8, 2026