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Skinergy Plus

FDA UDI

Class I (US FDA UDI)

by Hugh Steeper Limited

Identity

Trade Name
Skinergy Plus FDA UDI
Generic Name
External limb prosthesis finishing component, non-customized FDA UDI
Model / Reference
Closed Toe TrueFinish™ Skinergy Plus 22/23 Left Large Colour E3 FDA UDI

Identifiers

Catalog Number
TNS22LL/E3 FDA UDI
Primary DI / UDI-DI
05055348232861 FDA UDI
FDA Product Code
IPM FDA UDI
GMDN Term
External limb prosthesis finishing component, non-customized FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: External limb prosthesis finishing component, non-customized

Skinergy Plus by Hugh Steeper Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External limb prosthesis finishing component, non-customized.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hugh Steeper Limited

Sources (1)

  • FDA UDI cd8c9a11-2cf9-4957-8303-984887e27cc8 33 fields · synced May 31, 2026