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Aequalis™ Flex Revive™

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
AEQUALIS™ FLEX REVIVE™ FDA UDI
Generic Name
Coated shoulder humeral stem prosthesis FDA UDI
Model / Reference
ARS980910 FDA UDI

Identifiers

Catalog Number
ARS980910 FDA UDI
Primary DI / UDI-DI
00846832074419 FDA UDI
FDA Product Code
HSD FDA UDI
KWS FDA UDI
PHX FDA UDI
GMDN Term
Coated 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
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
Length — 130 Millimeter FDA UDI
Outer Diameter — 15 Millimeter FDA UDI

Category: Coated shoulder humeral stem prosthesis

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

Similar devices

Also classified as Coated shoulder humeral stem prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI c846e261-4d51-4ad2-bad6-b8276b653771 35 fields · synced May 31, 2026