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Iq

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
IQ FDA UDI
Generic Name
Surgical instrument interim-placement holder, reusable FDA UDI
Device Name
IQ TRAY TIBIA EXTENSION STEMS FDA UDI
Model / Reference
NS818R FDA UDI
Description
IQ TRAY TIBIA EXTENSION STEMS FDA UDI

Identifiers

Catalog Number
NS818R FDA UDI
Primary DI / UDI-DI
04046964026898 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Surgical instrument interim-placement holder, reusable 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument interim-placement holder, reusable

Iq by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument interim-placement holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 9df92fe7-875f-4fd7-83b8-f672d971885d 35 fields · synced May 30, 2026