Exact Reverse Fp Full Tooth Rasp

FDA UDI

Class I (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name: EXACT REVERSE FP FULL TOOTH RASP FDA UDI
Generic Name: Femoral stem prosthesis trial FDA UDI
Model / Reference: SSI005614 FDA UDI

Identifiers

Catalog Number: SSI005614 FDA UDI
Primary DI / UDI-DI: 00889024584914 FDA UDI
FDA Product Code: HTR FDA UDI
GMDN Term: Femoral stem prosthesis trial 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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Femoral stem prosthesis trial

Exact Reverse Fp Full Tooth Rasp by Zimmer, 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: Zimmer, Inc.

Sources (1)

FDA UDI 9b6b4531-ffff-4127-8971-af9f26eb1841 35 fields · synced May 30, 2026