Instrument, Manual, Surgical, General Use

FDA UDI

Class I (US FDA UDI)

by Parcus Medical Llc

Identity

Trade Name: INSTRUMENT, MANUAL, SURGICAL, GENERAL USE FDA UDI
Generic Name: Surgical mallet FDA UDI
Device Name: Mallet FDA UDI
Model / Reference: 10559 FDA UDI
Description: Mallet FDA UDI

Identifiers

Primary DI / UDI-DI: 00816342021531 FDA UDI
FDA Product Code: MDM FDA UDI
GMDN Term: Surgical mallet FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical mallet

Instrument, Manual, Surgical, General Use by Parcus Medical Llc — 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: Parcus Medical Llc

Sources (1)

FDA UDI 5166579a-2478-4cf1-b791-fca594cd00b4 33 fields · synced Jun 8, 2026