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Ocean Pacific NeoNatural

FDA UDI

Class I (US FDA UDI)

by AMD Medicom Inc

Identity

Trade Name
Ocean Pacific NeoNatural FDA UDI
Generic Name
Polychloroprene examination/treatment glove, non-powdered FDA UDI
Device Name
Ocean Pacific NeoNatural - Polychloroprene Medical Examination Gloves - Chemotherapy Tested - Textured Fingertips - Powder Free - Non-Sterile - Chemical Resistant Emerald - Small FDA UDI
Model / Reference
1228-B FDA UDI
Description
Ocean Pacific NeoNatural - Polychloroprene Medical Examination Gloves - Chemotherapy Tested - Textured Fingertips - Powder Free - Non-Sterile - Chemical Resistant Emerald - Small FDA UDI

Identifiers

Catalog Number
1228-B FDA UDI
Primary DI / UDI-DI
10686864056055 FDA UDI
510(k) Number
K040607 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Polychloroprene examination/treatment glove, non-powdered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polychloroprene examination/treatment glove, non-powdered

Ocean Pacific NeoNatural by AMD Medicom Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polychloroprene examination/treatment glove, non-powdered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AMD Medicom Inc

Sources (1)

  • FDA UDI 04fdc1dd-2915-47dd-802c-f9e63de4167b 38 fields · synced Jun 6, 2026