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Rhino Rescue

FDA UDI

Class I (US FDA UDI)

by Wuxi Emsrun Technology Co., Ltd.

Identity

Trade Name
RHINO RESCUE FDA UDI
Generic Name
First aid limb splint, non-mouldable, single-use FDA UDI
Model / Reference
CPPRJB0005 FDA UDI

Identifiers

Primary DI / UDI-DI
16974567745906 FDA UDI
FDA Product Code
HSP FDA UDI
GMDN Term
First aid limb splint, non-mouldable, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5890 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: First aid limb splint, non-mouldable, single-use

Rhino Rescue by Wuxi Emsrun Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid limb splint, non-mouldable, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wuxi Emsrun Technology Co., Ltd.

Sources (1)

  • FDA UDI 284165e1-ec2d-49f7-ad7c-caca1a34b4da 32 fields · synced May 30, 2026