← Back to catalogue

Aequalis

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
AEQUALIS FDA UDI
Generic Name
Uncoated shoulder humeral stem prosthesis FDA UDI
Model / Reference
DWB562 FDA UDI

Identifiers

Catalog Number
DWB562 FDA UDI
Primary DI / UDI-DI
03700386915611 FDA UDI
FDA Product Code
HSD FDA UDI
KWS FDA UDI
GMDN Term
Uncoated shoulder humeral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3660 FDA UDI
Commercial Distribution
Not 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 — 6.5 Millimeter FDA UDI
Angle — 130 degree FDA UDI
Length — 147 Millimeter FDA UDI

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

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 04027884-9cda-40a8-8ad8-241f6dd5e785 36 fields · synced Jun 1, 2026