Life Instruments

FDA UDI

Class I (US FDA UDI)

by Life Instrument Corporation

Identity

Trade Name: Life Instruments FDA UDI
Generic Name: Spinal rongeur FDA UDI
Device Name: Ferris Smith Pituitary Rongeur (Set of 4) 2-5mm FDA UDI
Model / Reference: 831-1000-4 FDA UDI
Description: Ferris Smith Pituitary Rongeur (Set of 4) 2-5mm FDA UDI

Identifiers

Primary DI / UDI-DI: M930831100040 FDA UDI
FDA Product Code: HTX FDA UDI
GMDN Term: Spinal rongeur FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 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

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

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Spinal rongeur

Life Instruments by Life Instrument Corporation — 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: Life Instrument Corporation

Sources (1)

FDA UDI 22efdf02-e8c9-447c-aa29-58755eee0dcf 33 fields · synced May 29, 2026