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Advocate Lancets Pull Top 30 Gauge

FDA UDI

Class II (US FDA UDI)

by Diabetic Supply Of Suncoast, Inc.

Identity

Trade Name
Advocate Lancets Pull Top 30 Gauge FDA UDI
Generic Name
Blood lancet, single-use FDA UDI
Device Name
Advocate Lancets Pull Top 30 Gauge Box 100, sterile, fine gauge, tri-bevel for obtaining virtually painless capillary blood sample, consistent depth penetration, universal design fits almost all lancing devices, pull off protective cap, discard lancet in puncture-resistant container. FDA UDI
Model / Reference
307 FDA UDI
Description
Advocate Lancets Pull Top 30 Gauge Box 100, sterile, fine gauge, tri-bevel for obtaining virtually painless capillary blood sample, consistent depth penetration, universal design fits almost all lancing devices, pull off protective cap, discard lancet in puncture-resistant container. FDA UDI

Identifiers

Primary DI / UDI-DI
00894046001066 FDA UDI
FDA Product Code
FMK 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood lancet, single-use

Advocate Lancets Pull Top 30 Gauge by Diabetic Supply Of Suncoast, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood lancet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI afa946e0-f13d-4571-bab0-d2aebbd2c06b 34 fields · synced Jun 6, 2026