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Bjingles

FDA UDI

Class II (US FDA UDI)

by Nk American Way, Llc

Identity

Trade Name
Bjingles FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Device Name
Infrared Thermometer FDA UDI
Model / Reference
BJL-995 FDA UDI
Description
Infrared Thermometer FDA UDI

Identifiers

Catalog Number
BJL-995 FDA UDI
Primary DI / UDI-DI
00861910000340 FDA UDI
510(k) Number
K171214 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, skin 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Infrared patient thermometer, skin

Bjingles by Nk American Way, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, skin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5758f220-be97-4ef4-9e63-ffc4c164bc59 35 fields · synced Jun 6, 2026