← Back to catalogue

Aequalis Reversed

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
AEQUALIS REVERSED FDA UDI
Generic Name
Total reverse shoulder prosthesis FDA UDI
Model / Reference
DWE045 FDA UDI

Identifiers

Catalog Number
DWE045 FDA UDI
Primary DI / UDI-DI
03700386936531 FDA UDI
FDA Product Code
HSD FDA UDI
KWS FDA UDI
PHX FDA UDI
GMDN Term
Total reverse shoulder prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 9 Millimeter FDA UDI
Length — 100 Millimeter FDA UDI

Category: Total reverse shoulder prosthesis

Aequalis Reversed by Tornier, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total reverse shoulder prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI e3d913e8-3de6-40d8-832e-e3e15212791e 35 fields · synced May 30, 2026