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Headgear

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ESH0101002Model CP611001、CP611002

by Xiamen Compower Medical Tech. Co., Ltd.

Identity

Trade Name
Headgear EUDAMED
Compower FDA UDI
Generic Name
Anaesthesia mask strap, single-use FDA UDI
Device Name
Headgear EUDAMED
Headgear is designed to fit the mask over the patient 's hand. FDA UDI
Model / Reference
CP611001、CP611002 EUDAMED
ESH0101002 EUDAMED
CP611002 FDA UDI
Description
Headgear is designed to fit the mask over the patient 's hand. FDA UDI

Identifiers

Primary DI / UDI-DI
06946430423313 EUDAMEDFDA UDI
Basic UDI-DI
694643043889515UF EUDAMED
FDA Product Code
BTK FDA UDI
EMDN Code
R9080 RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED
GMDN Term
Anaesthesia mask strap, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.5560 FDA UDI
Market of Registration
Sweden 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gas-sampling/monitoring respiratory tubing, single-use

Headgear by Xiamen Compower Medical Tech. Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000011703
Authorised Representative
Sungo Cert GmbH DE-AR-000010869

Sources (2)

  • EUDAMED f8ff1e82-ac26-40f2-9cbd-a2528fd11bf5 61 fields · synced Jul 10, 2026
  • FDA UDI 71832f61-8b38-403d-8781-ac3ff4c48e57 33 fields · synced May 30, 2026