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Sampedro

FDA UDI

Class II (US FDA UDI)

by Industrias Medicas Sampedro S.A.S

Identity

Trade Name
SAMPEDRO FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable, non-sterile FDA UDI
Device Name
Lateral Proximal Tibia Plate -2H - Right FDA UDI
Model / Reference
0 FDA UDI
Description
Lateral Proximal Tibia Plate -2H - Right FDA UDI

Identifiers

Catalog Number
PTPLD02 FDA UDI
Primary DI / UDI-DI
07708434060425 FDA UDI
510(k) Number
K220199 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable, non-sterile FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

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 fixation plate, non-bioabsorbable, non-sterile

Sampedro by Industrias Medicas Sampedro S.A.S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 379f5d3a-a013-4f63-950d-308385868fbc 35 fields · synced Jun 8, 2026