Skip to content

Punch BOX 9570970

by Mc Bio SRL

Punch BOX 9570970 is a Class I device made by Mc Bio SRL, listed in FDA GUDID since 1 Sep 2026 (UDI-DI 08057639712929), 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 Number08057639712929 UDI-DI Date1 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  • Withdrawn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
Punch BOX
Generic name
Instrument tray, reusable
Model / reference
9570970
Primary DI / UDI-DI
08057639712929
FDA product code
LRP
GMDN term
Instrument tray, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code LRP (Tray, Surgical).

Other devices from Mc Bio SRL

See all devices from Mc Bio SRL →

Properties

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