← Back to catalogue

Sterizign Sterilization Tray

FDA UDI

Class II (US FDA UDI)

by Sterizign Precision Technologies, LLC

Identity

Trade Name
Sterizign Sterilization Tray FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
standard tray 10x10x2 inches FDA UDI
Model / Reference
STER10x10x2 FDA UDI
Description
standard tray 10x10x2 inches FDA UDI

Identifiers

Catalog Number
STER10x10x2 FDA UDI
Primary DI / UDI-DI
G476STER10X10X2 FDA UDI
510(k) Number
K171520 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 2 Inch FDA UDI
Length — 10 Inch FDA UDI
Width — 10 Inch FDA UDI

Category: Device sterilization/disinfection container, reusable

Sterizign Sterilization Tray by Sterizign Precision Technologies, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, 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

Sources (1)

  • FDA UDI 848a8402-60d7-4e65-8e22-3c09ae94a155 37 fields · synced May 30, 2026