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Rhino Rescue

EUDAMEDFDA UDI

Class I (EU MDR)

Ref HFCG01Model HFEB01

by Anji Hengfeng Sanitary Material Co., Ltd

Identity

Trade Name
Rhino Rescue EUDAMEDFDA UDI
Generic Name
Woven gauze roll/sheet FDA UDI
Device Name
Sterile Bandage EUDAMED
Model / Reference
HFEB01 EUDAMED
HFCG01 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
06971519616706 EUDAMEDFDA UDI
Basic UDI-DI
697151961HFEB01EU EUDAMED
FDA Product Code
NAB FDA UDI
EMDN Code
M03040199 ELASTIC COMPRESSION BANDAGES - OTHER EUDAMED
GMDN Term
Woven gauze roll/sheet FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4014 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Rhino Rescue by Anji Hengfeng Sanitary Material 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-000013051
Authorised Representative
Caretechion GmbH DE-AR-000005946

Sources (2)

  • EUDAMED 9b7f5dac-20c3-4575-aa7a-203965a18b1d 61 fields · synced Jul 16, 2026
  • FDA UDI 5946091f-3954-49c4-8e83-0a49787e3fa6 32 fields · synced May 30, 2026