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De Mayo Universal Distractor®

FDA UDI

Class I (US FDA UDI)

by Innovative Medical Products, Inc.

Identity

Trade Name
De Mayo Universal Distractor® FDA UDI
Generic Name
Orthopaedic surgical distractor, external FDA UDI
Device Name
DEMO De Mayo Universal Distractor® FDA UDI
Model / Reference
907-DEMO FDA UDI
Description
DEMO De Mayo Universal Distractor® FDA UDI

Identifiers

Catalog Number
907-DEMO FDA UDI
Primary DI / UDI-DI
00696588005027 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Orthopaedic surgical distractor, external FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

No

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: Orthopaedic surgical distractor, external

De Mayo Universal Distractor® by Innovative Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical distractor, external.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innovative Medical Products, Inc.

Sources (1)

  • FDA UDI 3b2e2d77-ecd8-4dc4-b5ab-c8f1d8099638 34 fields · synced May 30, 2026