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SmartPractice

FDA UDI

Class II (US FDA UDI)

by Smart Health Llc

Identity

Trade Name
SmartPractice FDA UDI
Generic Name
Biological sterilization indicator FDA UDI
Device Name
S/P BIO MONITOR MAIL 3 TEST *12 #SMP120 FDA UDI
Model / Reference
62099 FDA UDI
Description
S/P BIO MONITOR MAIL 3 TEST *12 #SMP120 FDA UDI

Identifiers

Catalog Number
62099 FDA UDI
Primary DI / UDI-DI
D766620991 FDA UDI
FDA Product Code
FRC FDA UDI
GMDN Term
Biological sterilization indicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Biological sterilization indicator

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

Similar devices

Also classified as Biological sterilization indicator.

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 7ada041e-1820-4a0c-9da7-e66cfb2e2862 35 fields · synced Jun 1, 2026