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Aesculap MF330R

by Aesculap, Inc.

Aesculap MF330R is a Class II device made by Aesculap, Inc., listed in FDA GUDID since 9 Mar 2019 (UDI-DI 04046964571572), 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 Number04046964571572 UDI-DI Date9 Mar 2019ListedStatusListed 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  • Withdrawn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
Aesculap
Generic name
Hand-held surgical retractor, reusable
Model / Ref / Catalog
MF330R
Primary DI / UDI-DI
04046964571572
FDA product code
GZT
GMDN term
Hand-held surgical retractor, reusable
Device class
Class II
Regulation number
882.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Hand-held surgical retractor, reusable

Similar devices in this category

Other devices filed under Hand-held surgical retractor, reusable.

Other devices from Aesculap, Inc.

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)