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EPIX AntiRotation Device

FDA UDI

Class II (US FDA UDI)

by Epix Orthopaedics Inc.

Identity

Trade Name
EPIX AntiRotation Device FDA UDI
Generic Name
Flexible intramedullary nail FDA UDI
Device Name
Intramedullary And Accessories FDA UDI
Model / Reference
3315-00000 FDA UDI
Description
Intramedullary And Accessories FDA UDI

Identifiers

Catalog Number
3315-00000 FDA UDI
Primary DI / UDI-DI
B2213315000001 FDA UDI
510(k) Number
K133104 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Flexible intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Flexible intramedullary nail

EPIX AntiRotation Device by Epix Orthopaedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible intramedullary nail.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9bbb04f2-3d27-4e97-8706-9d024f3711cc 36 fields · synced Jun 8, 2026