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Duckworth & Kent

FDA UDI

Class I (US FDA UDI)

by Duckworth And Kent Limited

Identity

Trade Name
Duckworth & Kent FDA UDI
Generic Name
Needle guide, reusable FDA UDI
Device Name
Injection Guide FDA UDI
Model / Reference
9-544-2 FDA UDI
Description
Injection Guide FDA UDI

Identifiers

Catalog Number
9-544-2 FDA UDI
Primary DI / UDI-DI
05055313827450 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Needle guide, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Needle guide, reusable

Duckworth & Kent by Duckworth And Kent Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needle guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Duckworth And Kent Limited

Sources (1)

  • FDA UDI 88cd0ed8-a58d-4c5c-a87b-c9cedf52c249 35 fields · synced May 30, 2026