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SmartPractice

FDA UDI

Class II (US FDA UDI)

by Smart Health Llc

Identity

Trade Name
SmartPractice FDA UDI
Generic Name
Surgical/medical respirator, non-antimicrobial, single-use FDA UDI
Device Name
MASK EARLP S/P FLUID RESIST PNK*50 #658-00311 FDA UDI
Model / Reference
SP440069 FDA UDI
Description
MASK EARLP S/P FLUID RESIST PNK*50 #658-00311 FDA UDI

Identifiers

Catalog Number
SP440069 FDA UDI
Primary DI / UDI-DI
D766SP4400691 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical respirator, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical/medical respirator, non-antimicrobial, single-use

SmartPractice by Smart Health Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical respirator, non-antimicrobial, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smart Health Llc

Sources (1)

  • FDA UDI 5c65fe24-e8a8-40f1-b09f-fd7fbc19143e 35 fields · synced May 30, 2026