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Foldaway Stretcher

EUDAMEDFDA UDI

Class I (EU MDR)

Ref YDC-1A1Model YDC-1A1,YDC-1A3,YDC-1A4,YDC-1A4H,YDC-1A5,YDC-1A6,YDC-1A7,YDC-1A9,YDC-1A10,YDC-1A11,YDC-1A12,YDC-1A13,YDC-1A14,YDC-1A16,YDC-1A17,YDC-1A22,YDC-1A23,YDC-1F1,YDC-1F2,YDC-1F3,CST-01,CST-05,RWS-68,RBS-11

by Jiangsu Rixin Medical Equipment Co., Ltd.

Identity

Trade Name
Foldaway Stretcher EUDAMED
RED LEAF FDA UDI
Generic Name
Portable stretcher FDA UDI
Device Name
Foldaway Stretcher EUDAMED
Model / Reference
YDC-1A1,YDC-1A3,YDC-1A4,YDC-1A4H,YDC-1A5,YDC-1A6,YDC-1A7,YDC-1A9,YDC-1A10,YDC-1A11,YDC-1A12,YDC-1A13,YDC-1A14,YDC-1A16,YDC-1A17,YDC-1A22,YDC-1A23,YDC-1F1,YDC-1F2,YDC-1F3,CST-01,CST-05,RWS-68,RBS-11 EUDAMED
YDC-1A1 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
06974442051118 EUDAMEDFDA UDI
Basic UDI-DI
697444205FS001CN EUDAMED
FDA Product Code
FPP FDA UDI
EMDN Code
V08050101 GENERIC USE STRETCHERS EUDAMED
GMDN Term
Portable stretcher FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.6900 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

Foldaway Stretcher by Jiangsu Rixin Medical Equipment 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-000008761
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED 55636c94-c552-43bd-9837-b1bcae168f28 61 fields · synced Jul 23, 2026
  • FDA UDI 4b98a57d-aa13-4865-966d-7023f90dba2d 32 fields · synced May 29, 2026