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SCL SP Applicator 9575120

by Mc Bio SRL

SCL SP Applicator 9575120 is a Class I device made by Mc Bio SRL, listed in FDA GUDID since 3 Sep 2026 (UDI-DI 08057639712783), 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 Number08057639712783 UDI-DI Date3 Sep 2026ListedStatusListed 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  • Withdrawn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
SCL SP Applicator
Generic name
Periosteal elevator, reusable
Model / reference
9575120
Primary DI / UDI-DI
08057639712783
FDA product code
EMJ
GMDN term
Periosteal elevator, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code EMJ (Elevator, Surgical, Dental).

Other devices from Mc Bio SRL

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)