Peg, 1.8mm

FDA UDI

Class II (US FDA UDI)

by Miami Device Solutions

Identity

Trade Name: Peg, 1.8mm FDA UDI
Generic Name: Orthopaedic bone screw (non-sliding) FDA UDI
Device Name: Peg, Ø1.8mm x L30mm FDA UDI
Model / Reference: MDS1902P30 FDA UDI
Description: Peg, Ø1.8mm x L30mm FDA UDI

Identifiers

Catalog Number: MDS1902P30 FDA UDI
Primary DI / UDI-DI: 10812269025291 FDA UDI
FDA Product Code: HWC FDA UDI
HRS FDA UDI
GMDN Term: Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3040 FDA UDI
888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 1.8 Millimeter FDA UDI
Length — 30 Millimeter FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Peg, 1.8mm by Miami Device Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

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PANGEA — Stryker Corp. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Miami Device Solutions

Sources (1)

FDA UDI 17bdbc8c-e6c4-4e4e-ae72-df030336ea56 36 fields · synced May 30, 2026