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TORNIER PERFORM™ Patient-Matched

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
TORNIER PERFORM™ Patient-Matched FDA UDI
Generic Name
Reverse shoulder prosthesis base plate FDA UDI
Model / Reference
DWJ607 FDA UDI

Identifiers

Catalog Number
DWJ607 FDA UDI
Primary DI / UDI-DI
00846832079520 FDA UDI
FDA Product Code
KWS FDA UDI
PHX FDA UDI
GMDN Term
Reverse shoulder prosthesis base plate FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 35 Millimeter FDA UDI
Outer Diameter — 25 Millimeter FDA UDI

Category: Reverse shoulder prosthesis base plate

TORNIER PERFORM™ Patient-Matched by Tornier, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reverse shoulder prosthesis base plate.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI 9a2b33c1-cf9a-45e1-a2b9-21d6e4cd1198 35 fields · synced May 30, 2026