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Manual Bed

EUDAMEDFDA UDI

Class I (EU MDR)

Ref N/AModel XFA-5

by Hebei Xingfang Medical Instruments Technology Co., Ltd

Identity

Trade Name
Xingfang FDA UDI
Generic Name
Manual hospital bed FDA UDI
Device Name
Manual Bed EUDAMED
Model / Reference
XFA-5 EUDAMEDFDA UDI
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
06975851430013 EUDAMEDFDA UDI
Basic UDI-DI
697585143ManualBed00127 EUDAMED
FDA Product Code
FNJ FDA UDI
EMDN Code
V080602 MANUAL MEDICAL BEDS EUDAMED
GMDN Term
Manual hospital bed FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5120 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Manual Bed by Hebei Xingfang Medical Instruments Technology Co., Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000028599
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED 8bb49540-a327-474a-81b6-512e9fb2bdb0 61 fields · synced Aug 4, 2026
  • FDA UDI 581f3292-dede-4dc8-8b00-dfc3657b03b7 32 fields · synced May 30, 2026