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Bigfoot Lancets 33 Gauge

FDA UDI

Class II (US FDA UDI)

by Bigfoot Biomedical, Inc.

Identity

Trade Name
Bigfoot Lancets 33 Gauge FDA UDI
Generic Name
Blood lancing device tip FDA UDI
Device Name
Bigfoot Lancets 33 Gauge, 100CT FDA UDI
Model / Reference
FG-300294 FDA UDI
Description
Bigfoot Lancets 33 Gauge, 100CT FDA UDI

Identifiers

Catalog Number
FG-300294 FDA UDI
Primary DI / UDI-DI
00850003506104 FDA UDI
FDA Product Code
FMK FDA UDI
GMDN Term
Blood lancing device tip 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood lancing device tip

Bigfoot Lancets 33 Gauge by Bigfoot Biomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood lancing device tip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d75e2e6-f436-46a9-9d21-0dcb07c134db 35 fields · synced Jun 8, 2026