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Minop FH630R

by Aesculap, Inc.

Minop FH630R is a Class I device made by Aesculap, Inc., listed in FDA GUDID since 24 Apr 2020 (UDI-DI 04046963832735), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046963832735 UDI-DI Date24 Apr 2020ListedStatusListed 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  • Withdrawn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
Minop
Generic name
Open-surgery dissector
Model / Ref / Catalog
FH630R
Primary DI / UDI-DI
04046963832735
FDA product code
GZX
GMDN term
Open-surgery dissector
Device class
Class I
Regulation number
882.4525
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery dissector

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties

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