← Back to catalogue

Sampedro

FDA UDI

Class I (US FDA UDI)

by Industrias Medicas Sampedro S.A.S

Identity

Trade Name
SAMPEDRO FDA UDI
Generic Name
Open-surgery dissector FDA UDI
Device Name
SharpHook FDA UDI
Model / Reference
0 FDA UDI
Description
SharpHook FDA UDI

Identifiers

Catalog Number
/EC155 FDA UDI
Primary DI / UDI-DI
07708604560106 FDA UDI
FDA Product Code
HWO FDA UDI
GMDN Term
Open-surgery dissector 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: Open-surgery dissector

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 Open-surgery dissector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 8b856f55-514b-43a7-b15e-a799313de181 34 fields · synced Jun 8, 2026