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Aequalis Reversed II

FDA UDI

Class I (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
Aequalis Reversed II FDA UDI
Generic Name
Drilling power tool attachment, basic FDA UDI
Device Name
USA DRILL BIT AND REAMER HOLDER FDA UDI
Model / Reference
MWB222 FDA UDI
Description
USA DRILL BIT AND REAMER HOLDER FDA UDI

Identifiers

Catalog Number
MWB222 FDA UDI
Primary DI / UDI-DI
03700386969522 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Drilling power tool attachment, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Drilling power tool attachment, basic

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

Similar devices

Also classified as Drilling power tool attachment, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI 7b7ea936-aece-4fd5-958a-8292f03ee720 35 fields · synced Jun 8, 2026