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: Toothed Pituitary Ronguer 3mm up FDA UDI
Model / Reference: 732-1230-1B FDA UDI
Description: Toothed Pituitary Ronguer 3mm up FDA UDI

Identifiers

Primary DI / UDI-DI: M93073212301B0 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

MRI Safety

MR Conditional 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 9c88a4a1-9204-405f-9297-c7fa7afe5e6a 33 fields · synced Jun 1, 2026