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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
Surgical mallet head FDA UDI
Device Name
Cottle mallet φ30mm FDA UDI
Model / Reference
0 FDA UDI
Description
Cottle mallet φ30mm FDA UDI

Identifiers

Catalog Number
/M30 FDA UDI
Primary DI / UDI-DI
07708626670173 FDA UDI
FDA Product Code
HXL FDA UDI
GMDN Term
Surgical mallet head FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Surgical mallet head

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 Surgical mallet head.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d403f25c-17df-4c0b-ae33-4eced9d52055 34 fields · synced May 29, 2026