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Sampedro

FDA UDI

Class I (US FDA UDI)

by Industrias Medicas Sampedro S.A.S

Identity

Trade Name
SAMPEDRO FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
Hohmann Retractor 28.5cm FDA UDI
Model / Reference
0 FDA UDI
Description
Hohmann Retractor 28.5cm FDA UDI

Identifiers

Catalog Number
/SH285 FDA UDI
Primary DI / UDI-DI
07708626670906 FDA UDI
FDA Product Code
HWO FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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: Orthopaedic inorganic implant inserter/extractor, reusable

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

Similar devices

Also classified as Orthopaedic inorganic implant inserter/extractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Industrias Medicas Sampedro S.A.S

Sources (1)

  • FDA UDI 8d27af01-8635-4bec-944e-6e909b9ee9fd 34 fields · synced Jun 1, 2026