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33cm Laparoscopic Curved Blade - PL 20106ACT

by Xodus Medical, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00787551002409 UDI-DI Date21 Apr 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
33cm Laparoscopic Curved Blade; Blue PTFE; Black Insulation; PL
Generic Name
Open-surgery electrosurgical electrode, monopolar, single-use
Model / Reference
20106ACT
Primary DI / UDI-DI
00787551002409
FDA Product Code
GEI
GMDN Term
Open-surgery electrosurgical electrode, monopolar, single-use
Models / Variants
PL 20106ACT
Device Class
Class II
Regulation Number
878.4400
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Related devices

Category: Open-surgery electrosurgical electrode, monopolar, single-use

Other devices from Xodus Medical, Inc.

See all devices from Xodus Medical, Inc. →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No
  • Manufacturing Date: No