← Back to catalogue

Pico

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew Medical, Ltd.

Identity

Trade Name
PICO FDA UDI
Generic Name
Negative-pressure wound therapy system, electric, single-use FDA UDI
Device Name
PICO 15cm x 20cm Dual Dressing Kit US FDA UDI
Model / Reference
66021362 FDA UDI
Description
PICO 15cm x 20cm Dual Dressing Kit US FDA UDI

Identifiers

Catalog Number
66021362 FDA UDI
Primary DI / UDI-DI
05000223491055 FDA UDI
FDA Product Code
OMP FDA UDI
GMDN Term
Negative-pressure wound therapy system, electric, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Negative-pressure wound therapy system, electric, single-use

Pico by Smith & Nephew Medical, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system, electric, single-use.

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

Manufacturer
Smith & Nephew Medical, Ltd.

Sources (1)

  • FDA UDI a79a3926-719a-4107-850c-6e5c7006daed 34 fields · synced May 29, 2026