← Back to catalogue

Inion S-1 instrument

FDA UDI

Class II (US FDA UDI)

by Inion , Ltd.

Identity

Trade Name
Inion S-1 instrument FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Sterilization tray for instruments FDA UDI
Model / Reference
1 FDA UDI
Description
Sterilization tray for instruments FDA UDI

Identifiers

Catalog Number
ACC-9841 FDA UDI
Primary DI / UDI-DI
M224ACC984110 FDA UDI
510(k) Number
K071810 FDA UDI
FDA Product Code
OJB FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Inion S-1 instrument by Inion , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Inion , Ltd.

Sources (1)

  • FDA UDI 00f0eb57-3f16-4e65-9ef4-0bb7c89bb26d 35 fields · synced Jun 1, 2026