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Diska Nulife

FDA UDI

Class I (US FDA UDI)

by Diska LLC

Identity

Trade Name
Diska Nulife FDA UDI
Generic Name
Stand-on floor scale, electronic FDA UDI
Device Name
Weight scale FDA UDI
Model / Reference
DNL-GBS-2104-G FDA UDI
Description
Weight scale FDA UDI

Identifiers

Primary DI / UDI-DI
00810115890799 FDA UDI
FDA Product Code
FRI FDA UDI
GMDN Term
Stand-on floor scale, electronic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2700 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Stand-on floor scale, electronic

Diska Nulife by Diska LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stand-on floor scale, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diska LLC

Sources (1)

  • FDA UDI 62f1171c-4c25-4e42-9b97-759d5cc92f8f 34 fields · synced Jun 8, 2026