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PremierPro

FDA UDI

Class II (US FDA UDI)

by Svs Llc

Identity

Trade Name
PremierPro FDA UDI
Generic Name
General-purpose patient temperature probe, reusable FDA UDI
Device Name
Digital Thermometer, Rectal, Bulk FDA UDI
Model / Reference
6802 FDA UDI
Description
Digital Thermometer, Rectal, Bulk FDA UDI

Identifiers

Primary DI / UDI-DI
00818566013330 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
General-purpose patient temperature probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 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

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

Yes

FDA UDI

Category: General-purpose patient temperature probe, reusable

PremierPro by Svs Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose patient temperature probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Svs Llc

Sources (1)

  • FDA UDI 04478d3a-6427-4689-a9bd-815ac6453991 34 fields · synced May 30, 2026