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Prodigy Combo Pre-Pack

FDA UDI

Class II (US FDA UDI)

by Prodigy Diabetes Care, Llc

Identity

Trade Name
Prodigy Combo Pre-Pack FDA UDI
Generic Name
Manual blood lancing device, reusable FDA UDI
Device Name
Prodigy Combo Pre-Pack 20 x Item # 073200; 5 x Item # 07120 FDA UDI
Model / Reference
075100 FDA UDI
Description
Prodigy Combo Pre-Pack 20 x Item # 073200; 5 x Item # 07120 FDA UDI

Identifiers

Catalog Number
075100 FDA UDI
Primary DI / UDI-DI
00384840751002 FDA UDI
FDA Product Code
NBW FDA UDI
CGA FDA UDI
GMDN Term
Manual blood lancing device, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose IVD, kit, electrometryManual blood lancing device, reusableHome-use/point-of-care blood glucose monitoring system IVD

Prodigy Combo Pre-Pack by Prodigy Diabetes Care, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home-use/point-of-care blood glucose monitoring system IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 64ffe1b4-5a55-4b56-ba66-ed547f0b3188 35 fields · synced May 31, 2026