Instrumentarium

FDA UDI

Class I (US FDA UDI)

by Société Chirurgicale Instrumentarium Inc

Identity

Trade Name: Instrumentarium FDA UDI
Generic Name: Luer/Luer linear connector, reusable FDA UDI
Model / Reference: 115.918.00 FDA UDI

Identifiers

Primary DI / UDI-DI: 00810055470952 FDA UDI
FDA Product Code: LRC FDA UDI
GMDN Term: Luer/Luer linear connector, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 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: Luer/Luer linear connector, reusable

Instrumentarium by Société Chirurgicale Instrumentarium 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: Société Chirurgicale Instrumentarium Inc

Sources (1)

FDA UDI 99c5d2bd-477f-449b-99d6-5e277ea478f2 32 fields · synced Jun 8, 2026