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CyberLAB

FDA UDI

Class I (US FDA UDI)

by Aspyra, Llc.

Identity

Trade Name
CyberLAB FDA UDI
Generic Name
Clinical laboratory information system application software FDA UDI
Device Name
Clinical Laboratory Information System application software FDA UDI
Model / Reference
7.3.1 FDA UDI
Description
Clinical Laboratory Information System application software FDA UDI

Identifiers

Catalog Number
CL731 FDA UDI
Primary DI / UDI-DI
B433CL0 FDA UDI
FDA Product Code
NVV FDA UDI
GMDN Term
Clinical laboratory information system application software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2100 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: Clinical laboratory information system application software

CyberLAB by Aspyra, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clinical laboratory information system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aspyra, Llc.

Sources (1)

  • FDA UDI 77cb06f0-ce29-475b-a36c-d0ad192e31c7 34 fields · synced Jun 1, 2026