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Sampedro 0

by Industrias Medicas Sampedro S.A.S 89 variants

Sampedro 0 (/PR135) is a Class I device made by Industrias Medicas Sampedro S.A.S, listed in FDA GUDID since 12 May 2022 (UDI-DI 07708604560748), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07708604560748 UDI-DI Date12 May 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sampedro
Generic name
Bone approximation clamp
Model / Ref / Catalog
0, /PR135
Primary DI / UDI-DI
07708604560748
FDA product code
HXK
GMDN term
Bone approximation clamp
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone approximation clamp

Similar devices in this category

Other devices filed under Bone approximation clamp.

Other devices from Industrias Medicas Sampedro S.A.S

  • Sampedro 0

    Class I

  • Sampedro 1

    Class II

  • Sampedro 0

    Class II

  • Sampedro 0

    Class II

See all devices from Industrias Medicas Sampedro S.A.S →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (9, all answered No)