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Skin Iq 1000

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref SIQCOBAS1UNModel 648305BG

by Arjohuntleigh, Inc.

Identity

Trade Name
SKIN IQ 1000 EUDAMEDFDA UDI
Generic Name
External circulating-air core temperature regulation system pad, single-use FDA UDI
Device Name
ALPHA ACTIVE 3 PUMP EUDAMED
Skin IQ 1000 - Mattress Coverlet FDA UDI
Model / Reference
SIQCOBAS1UN EUDAMEDFDA UDI
648305BG EUDAMED
Description
Skin IQ 1000 - Mattress Coverlet FDA UDI

Identifiers

Primary DI / UDI-DI
05055982783149 EUDAMEDFDA UDI
Basic UDI-DI
5060693520020VD EUDAMED
FDA Product Code
IOQ FDA UDI
EMDN Code
Z12019003 WOUND TREATMENT EQUIPMENT EUDAMED
GMDN Term
External circulating-air core temperature regulation system pad, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
890.5170 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: External circulating-air core temperature regulation system pad, single-use

Skin Iq 1000 by Arjohuntleigh, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as External circulating-air core temperature regulation system pad, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arjohuntleigh, Inc.

Sources (2)

  • FDA UDI d718c29e-833b-4b96-b438-34d6b727dbea 33 fields · synced Jun 19, 2026
  • EUDAMED 955ca62e-c198-43ca-b66d-edf6cf1fe342 61 fields · synced Jun 19, 2026