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Crutch

FDA UDI

Class I (US FDA UDI)

by Foshan Shunkangda Medical Tech Co., Ltd

Identity

Trade Name
Crutch FDA UDI
Generic Name
Single-base walking stick FDA UDI
Model / Reference
CA8012LS FDA UDI

Identifiers

Primary DI / UDI-DI
06972223254710 FDA UDI
FDA Product Code
IPR FDA UDI
GMDN Term
Single-base walking stick FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3150 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Single-base walking stick

Crutch by Foshan Shunkangda Medical Tech Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Single-base walking stick.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3f8e1315-bd8d-487f-8eb9-8c24b6208788 32 fields · synced May 30, 2026