PRACTIshield Sheath Props

FDA UDI

Class I (US FDA UDI)

by Practicon, Inc.

Identity

Trade Name: PRACTIshield Sheath Props FDA UDI
Generic Name: Needle recapping device, single-use FDA UDI
Device Name: With new, high-visibility target graphics, PRACTIshield slips onto any needle sheath, creating an effective prop for easier one-handed resheathing. Helps to remind and reinforce a safe technique. Puncture-resistant die-cut cardboard. 100 single-use shields per pack. FDA UDI
Model / Reference: 70-4970 FDA UDI
Description: With new, high-visibility target graphics, PRACTIshield slips onto any needle sheath, creating an effective prop for easier one-handed resheathing. Helps to remind and reinforce a safe technique. Puncture-resistant die-cut cardboard. 100 single-use shields per pack. FDA UDI

Identifiers

Catalog Number: 70-4970 FDA UDI
Primary DI / UDI-DI: 00723896009215 FDA UDI
FDA Product Code: DZM FDA UDI
GMDN Term: Needle recapping device, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4730 FDA UDI
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

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Needle recapping device, single-use

PRACTIshield Sheath Props by Practicon, Inc. — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Practicon, Inc.

Sources (1)

FDA UDI 9ad9879e-4566-47a5-bf0f-61df0e42f117 34 fields · synced May 29, 2026