VivaGuard Lancets (30G)

FDA UDI

Class II (US FDA UDI)

by ABOUND Diagnostics, Inc

Identity

Trade Name: VivaGuard Lancets (30G) FDA UDI
Generic Name: Blood lancet, single-use FDA UDI
Device Name: VivaGuard Lancets (30G) FDA UDI
Model / Reference: VGL01-383 FDA UDI
Description: VivaGuard Lancets (30G) FDA UDI

Identifiers

Catalog Number: VGL01-383 FDA UDI
Primary DI / UDI-DI: 00840423500110 FDA UDI
FDA Product Code: FMK FDA UDI
QRL FDA UDI
QRK FDA UDI
GMDN Term: Blood lancet, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood lancet, single-use

VivaGuard Lancets (30G) by ABOUND Diagnostics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood lancet, single-use.

Contact Activated Safety Lancet — NINGBO MEDSUN MEDICAL CO., LTD. · Class IIa
TysonBio — Shandong Lianfa Medical Plastic Products CO., LTD · Class II
McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
Safety Lancet (25G) — Shandong Lianfa Medical Plastic Products CO., LTD · Class II
Safety Lancet (23G) — Shandong Lianfa Medical Plastic Products CO., LTD · Class II
STERiLANCE — Sterilance Medical (Suzhou) Inc. · Class IIa
Lite3 — Sterilance Medical (Suzhou) Inc. · Class IIa
DropSafe Medlance Plus, safety lancets — HTL STREFA S A · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: ABOUND Diagnostics, Inc

Sources (1)

FDA UDI f6712c8f-db53-4d70-b1d7-c59b754f3689 35 fields · synced Jun 1, 2026