Ultilet 30g Classic Twist Lancet

FDA UDI

Class II (US FDA UDI)

by Boca Med, LLC

Identity

Trade Name: Ultilet 30g Classic Twist Lancet FDA UDI
Generic Name: Blood lancing device tip FDA UDI
Device Name: Ultilet 30g TwistTop Blood Lancet NDC Number: 08326-3010-01 FDA UDI
Model / Reference: 30101 FDA UDI
Description: Ultilet 30g TwistTop Blood Lancet NDC Number: 08326-3010-01 FDA UDI

Identifiers

Primary DI / UDI-DI: 10743820301014 FDA UDI
FDA Product Code: QRL 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

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

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood lancing device tip

Ultilet 30g Classic Twist Lancet by Boca Med, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Boca Med, LLC

Sources (1)

FDA UDI 8018b127-5bc0-4a7d-bc39-0f29b47c4aa0 33 fields · synced May 31, 2026