Sterrad

FDA UDI

Class I (US FDA UDI)

by Advanced Sterilization Products Services Inc.

Identity

Trade Name: Sterrad FDA UDI
Generic Name: Instrument tray, reusable FDA UDI
Device Name: Instrument Tray Mats 356 mm X 241 mm (14 in. x 9.5 in.) FDA UDI
Model / Reference: 99208 FDA UDI
Description: Instrument Tray Mats 356 mm X 241 mm (14 in. x 9.5 in.) FDA UDI

Identifiers

Catalog Number: 99208 FDA UDI
Primary DI / UDI-DI: 10705037043033 FDA UDI
FDA Product Code: FSM FDA UDI
GMDN Term: Instrument tray, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Instrument tray, reusable

Sterrad by Advanced Sterilization Products Services 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: Advanced Sterilization Products Services Inc.

Sources (1)

FDA UDI 0e1cf0f7-cd33-412b-bb01-a02d4a77e55d 36 fields · synced May 29, 2026