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Aesculap PL771SU

by Aesculap AG

Aesculap PL771SU is a Class II device made by Aesculap AG, listed in FDA GUDID since 15 Feb 2020 (UDI-DI 04046964837340), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046964837340 UDI-DI Date15 Feb 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  • Withdrawn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
Aesculap
Generic name
Endoscopic electrosurgical handpiece/electrode, bipolar, single-use
Model / Ref / Catalog
PL771SU
Primary DI / UDI-DI
04046964837340
FDA product code
GEI
GMDN term
Endoscopic electrosurgical handpiece/electrode, bipolar, single-use
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Similar devices in this category

Other devices filed under Endoscopic electrosurgical handpiece/electrode, bipolar, single-use.

Other devices from Aesculap AG

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)