← Back to catalogue

Advocate Lancets Safety 26 G 1.8 mm

FDA UDI

Class II (US FDA UDI)

by Diabetic Supply Of Suncoast, Inc.

Identity

Trade Name
Advocate Lancets Safety 26 G 1.8 mm FDA UDI
Generic Name
Manual blood lancing device, single-use FDA UDI
Device Name
Advocate Lancets Safety 26 G 1.8 mm, box of 100, sterile for capillary blood sample, needle automatically retracts, ready to use, no loading needed, single use only FDA UDI
Model / Reference
636 FDA UDI
Description
Advocate Lancets Safety 26 G 1.8 mm, box of 100, sterile for capillary blood sample, needle automatically retracts, ready to use, no loading needed, single use only FDA UDI

Identifiers

Primary DI / UDI-DI
00894046001929 FDA UDI
FDA Product Code
FMK FDA UDI
GMDN Term
Manual blood lancing device, 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual blood lancing device, single-use

Advocate Lancets Safety 26 G 1.8 mm 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, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI bc399372-4aa7-4a6a-af4c-88599f8441e7 34 fields · synced May 30, 2026