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Nordent Manufacturing Inc

FDA UDI

Class I (US FDA UDI)

by Nordent Manufacturing Inc

Identity

Trade Name
NORDENT MANUFACTURING INC FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
CASSETTE DUAL SIDED, MEDIUM STAINLESS STEEL WITH DIVIDER, 8 INSTRUMENTS, PURPLE, 5 1/2" X 8" FDA UDI
Model / Reference
CD2-8D7 FDA UDI
Description
CASSETTE DUAL SIDED, MEDIUM STAINLESS STEEL WITH DIVIDER, 8 INSTRUMENTS, PURPLE, 5 1/2" X 8" FDA UDI

Identifiers

Primary DI / UDI-DI
00840018646520 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Instrument tray, reusable

Nordent Manufacturing Inc by Nordent Manufacturing Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a596f065-0df3-4084-89f5-8ac4cfbe7ff9 33 fields · synced May 30, 2026