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ADVOCATE Lancing Device Red Dot

FDA UDI

Class II (US FDA UDI)

by Diabetic Supply Of Suncoast, Inc.

Identity

Trade Name
ADVOCATE Lancing Device Red Dot FDA UDI
Generic Name
Manual blood lancing device, reusable FDA UDI
Device Name
Advocate Lancing Device Red Dot, ergonomically designed, safety switch feature locks the trigger when uncapped, 6 depth adjustment, safer, easier lancet ejection FDA UDI
Model / Reference
329 FDA UDI
Description
Advocate Lancing Device Red Dot, ergonomically designed, safety switch feature locks the trigger when uncapped, 6 depth adjustment, safer, easier lancet ejection FDA UDI

Identifiers

Catalog Number
329 FDA UDI
Primary DI / UDI-DI
00852982006002 FDA UDI
FDA Product Code
FMK FDA UDI
GMDN Term
Manual blood lancing device, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4850 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual blood lancing device, reusable

ADVOCATE Lancing Device Red Dot by Diabetic Supply Of Suncoast, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual blood lancing device, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3a14fbd7-fc98-4ee6-88a0-2adac2899359 35 fields · synced May 30, 2026