Pip

FDA UDI

by Amity Holdings, Llc

Identity

Trade Name: PIP FDA UDI
Generic Name: Blood lancet, single-use FDA UDI
Device Name: PIP Trial Pack: 30ea 903; 10ea 901; 10ea 902 FDA UDI
Model / Reference: 903TP FDA UDI
Description: PIP Trial Pack: 30ea 903; 10ea 901; 10ea 902 FDA UDI

Identifiers

Catalog Number: 903TP FDA UDI
Primary DI / UDI-DI: 60732671609030 FDA UDI
GMDN Term: Blood lancet, single-use FDA UDI

Classification

Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

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

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Needle Gauge — 28 Gauge FDA UDI
Length — 1.8 Millimeter FDA UDI
Length — 1.0 Millimeter FDA UDI
Length — 1.6 Millimeter FDA UDI
Needle Gauge — 30 Gauge FDA UDI

Category: Blood lancet, single-use

Pip by Amity Holdings, Llc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Blood lancet, single-use.

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DropSafe Medlance Plus, safety lancets — HTL STREFA S A · Class II

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	N/A	Pending data

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Manufacturer

Manufacturer: Amity Holdings, Llc

Sources (1)

FDA UDI 4d8d46c5-6599-49f4-96dc-402bf70ff6bb 37 fields · synced Jun 1, 2026