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Stratum

FDA UDI

Class II (US FDA UDI)

by Medartis Inc.

Identity

Trade Name
Stratum FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
STRM MDS Screw 3.5x30mm ST FDA UDI
Model / Reference
STRM-MDS-3530ST FDA UDI
Description
STRM MDS Screw 3.5x30mm ST FDA UDI

Identifiers

Primary DI / UDI-DI
00817701023074 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

Category: Orthopaedic bone screw (non-sliding)

Stratum by Medartis Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medartis Inc.

Sources (1)

  • FDA UDI 1e9c73a2-7556-4561-b16d-4012efc35ff0 33 fields · synced May 31, 2026