Skip to content

Snowden-Pencer SP8495

by Steris Corporation

Snowden-Pencer SP8495 is a Class II device made by Steris Corporation, listed in FDA GUDID since 17 Oct 2017 (UDI-DI 10885403238529), 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 Number10885403238529 UDI-DI Date17 Oct 2017ListedStatusListed 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  • Withdrawn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
Snowden-Pencer
Generic name
Endoscopic electrosurgical electrode, monopolar, reusable
Model / Ref / Catalog
SP8495
Primary DI / UDI-DI
10885403238529
FDA product code
GCJ
GMDN term
Endoscopic electrosurgical electrode, monopolar, reusable
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscopic electrosurgical electrode, monopolar, reusable

Similar devices in this category

Other devices filed under Endoscopic electrosurgical electrode, monopolar, reusable.

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

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