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Dermacare

FDA UDI

Class I (US FDA UDI)

by Ehob, Inc.

Identity

Trade Name
DERMACARE FDA UDI
Generic Name
Freestanding patient positioner, single-use FDA UDI
Device Name
SINGLE 6X12X18 SMALL ABDUCTION PILL FDA UDI
Model / Reference
REV00 FDA UDI
Description
SINGLE 6X12X18 SMALL ABDUCTION PILL FDA UDI

Identifiers

Catalog Number
DC400302010 FDA UDI
Primary DI / UDI-DI
10603354500638 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Freestanding patient positioner, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 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

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

No

FDA UDI

Category: Freestanding patient positioner, single-use

Dermacare by Ehob, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ehob, Inc.

Sources (1)

  • FDA UDI 4c0e35c0-fba2-48bc-b960-1f95cde5d42a 34 fields · synced Jun 1, 2026