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Silvercrest

FDA UDI

Class II (US FDA UDI)

by Lidl Us, Llc

Identity

Trade Name
Silvercrest FDA UDI
Generic Name
Infrared patient thermometer, ear FDA UDI
Device Name
SFT81Multi-Purpose Thermometer FDA UDI
Model / Reference
IAN 387870_2101 FDA UDI
Description
SFT81Multi-Purpose Thermometer FDA UDI

Identifiers

Catalog Number
793.99 FDA UDI
Primary DI / UDI-DI
04055334330084 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, ear 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

Yes

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: Infrared patient thermometer, ear

Silvercrest by Lidl Us, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, ear.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lidl Us, Llc

Sources (1)

  • FDA UDI 910d118b-6018-48e5-b31c-b3d76d40c4d0 34 fields · synced May 30, 2026