Exmoor

FDA UDI

Class I (US FDA UDI)

by Exmoor Plastics , Ltd.

Identity

Trade Name: EXMOOR FDA UDI
Generic Name: General-purpose syringe, single-use FDA UDI
Device Name: Cream Ointment Ear Syringe FDA UDI
Model / Reference: L1 FDA UDI
Description: Cream Ointment Ear Syringe FDA UDI

Identifiers

Catalog Number: L1 FDA UDI
Primary DI / UDI-DI: 05060180256319 FDA UDI
FDA Product Code: LRD FDA UDI
GMDN Term: General-purpose syringe, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.5220 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose syringe, single-use

Exmoor by Exmoor Plastics , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, single-use.

Merit Medical® — Merit Medical Systems, Inc. · Class II
SOFT-JECT® — Henke-Sass, Wolf GmbH · Class II
CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
SURGYCO — Surgyco LLC · Class I
NAMIC — MEDLINE INDUSTRIES, INC. · Class II
HSW HENKE-JECT® — Henke-Sass, Wolf GmbH · Class II
BD Safety-Lok — BECTON DICKINSON AND COMPANY · Class II
SURGYCO — Surgyco LLC · Class I

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

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

Manufacturer

Manufacturer: Exmoor Plastics , Ltd.

Sources (1)

FDA UDI 92eef40a-dc21-4cc5-8f5f-7b46a20d6731 36 fields · synced May 30, 2026