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Dp4

FDA UDI

Class II (US FDA UDI)

by Equipmed USA B.V.

Identity

Trade Name
Dp4 FDA UDI
Generic Name
Medical equipment handle cover, single-use FDA UDI
Device Name
Device Sleeve - Box of 33 FDA UDI
Model / Reference
DP4-SLEEVE-USC-33-1 FDA UDI
Description
Device Sleeve - Box of 33 FDA UDI

Identifiers

Primary DI / UDI-DI
08720261027074 FDA UDI
FDA Product Code
QAI FDA UDI
GMDN Term
Medical equipment handle cover, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4430 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical equipment handle cover, single-use

Dp4 by Equipmed USA B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment handle cover, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Equipmed USA B.V.

Sources (1)

  • FDA UDI 43375869-aebc-4c38-809b-f4d418cde316 33 fields · synced May 31, 2026