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De Soutter Medical

FDA UDI

Class I (US FDA UDI)

by De Soutter Medical, Ltd.

Identity

Trade Name
De Soutter Medical FDA UDI
Generic Name
Bone/joint surgical power tool motorized handpiece/set, pneumatic FDA UDI
Device Name
DPX-170 OSCILLATING SAW HANDPIECE FDA UDI
Model / Reference
223224 FDA UDI
Description
DPX-170 OSCILLATING SAW HANDPIECE FDA UDI

Identifiers

Catalog Number
223224 FDA UDI
Primary DI / UDI-DI
05051471038820 FDA UDI
FDA Product Code
GET FDA UDI
GMDN Term
Bone/joint surgical power tool motorized handpiece/set, pneumatic 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone/joint surgical power tool motorized handpiece/set, pneumatic

De Soutter Medical by De Soutter Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone/joint surgical power tool motorized handpiece/set, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
De Soutter Medical, Ltd.

Sources (1)

  • FDA UDI 1abd39d5-15a3-4234-bbaf-006c9079d0c4 34 fields · synced Jun 8, 2026