Fisherbrand

FDA UDI

Class II (US FDA UDI)

by Fisher Scientific Company L.l.c.

Identity

Trade Name: Fisherbrand FDA UDI
Generic Name: Blood lancet, single-use FDA UDI
Device Name: FB LANCET 2.2MM 21G PNK 100/PK FDA UDI
Model / Reference: SC-220-100 FDA UDI
Description: FB LANCET 2.2MM 21G PNK 100/PK FDA UDI

Identifiers

Catalog Number: 13500102 FDA UDI
Primary DI / UDI-DI: 00613647010921 FDA UDI
510(k) Number: K221783 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood lancet, single-use

Fisherbrand by Fisher Scientific Company L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K221783 also covers:

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

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Manufacturer

Manufacturer: Fisher Scientific Company L.l.c.

Sources (1)

FDA UDI 976b6a70-9bce-4351-9421-f0774fb1e950 36 fields · synced May 30, 2026