← Back to catalogue

Glucertain

FDA UDI

Class II (US FDA UDI)

by CellEra, LLC

Identity

Trade Name
Glucertain FDA UDI
Generic Name
Manual blood lancing device, single-use FDA UDI
Device Name
Safety Lancet, 28 ga., 100/box, 10 boxes/case FDA UDI
Model / Reference
30228 FDA UDI
Description
Safety Lancet, 28 ga., 100/box, 10 boxes/case FDA UDI

Identifiers

Catalog Number
30228 FDA UDI
Primary DI / UDI-DI
00850031608115 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

Glucertain by CellEra, LLC — 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

Manufacturer
CellEra, LLC

Sources (1)

  • FDA UDI a641c917-2a78-4799-9bc2-f0a127dde5e8 35 fields · synced May 30, 2026