Ekcomed

FDA UDI

Class I (US FDA UDI)

by Ekcomed Inc.

Identity

Trade Name: EKCOMED FDA UDI
Generic Name: Limb/torso/head restraint, single-use FDA UDI
Device Name: Perineal Post Roll FDA UDI
Model / Reference: EKM-PPR0634 FDA UDI
Description: Perineal Post Roll FDA UDI

Identifiers

Catalog Number: EKM-PPR0634 FDA UDI
Primary DI / UDI-DI: 00850000965133 FDA UDI
FDA Product Code: CCX FDA UDI
GMDN Term: Limb/torso/head restraint, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.6820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Limb/torso/head restraint, single-use

Ekcomed by Ekcomed Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

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Manufacturer

Manufacturer: Ekcomed Inc.

Sources (1)

FDA UDI e31d9f5b-b3d1-4dbf-8b1f-581c23b778a9 35 fields · synced May 30, 2026