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Post Operative Carpal Sleeve, Small Right

FDA UDI

Class I (US FDA UDI)

by SILIPOS Holding LLC

Identity

Trade Name
Post Operative Carpal Sleeve, Small Right FDA UDI
Generic Name
Wrist orthosis FDA UDI
Model / Reference
14125 FDA UDI

Identifiers

Primary DI / UDI-DI
00614464141256 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Wrist orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wrist orthosis

Post Operative Carpal Sleeve, Small Right by SILIPOS Holding LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wrist orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SILIPOS Holding LLC

Sources (1)

  • FDA UDI e85656d6-539e-4fda-8802-2d0407a668b7 32 fields · synced May 30, 2026