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Blunt Dissector PS3886

by Purple Surgical International Limited

Blunt Dissector PS3886 is a dissection sponge (FDA Class I; FDA product code GDI, Dissector, Surgical, General & Plastic Surgery) made by Purple Surgical International Limited, listed in FDA GUDID since 17 Sep 2016 (UDI-DI 05051223004233), 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 Number05051223004233 UDI-DI Date17 Sep 2016ListedStatusListed 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  • Withdrawn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
Blunt Dissector
Generic name
Dissection sponge
Model / Ref / Catalog
PS3886
Primary DI / UDI-DI
05051223004233
FDA product code
GDI
GMDN term
Dissection sponge
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Size
Length — 400 Millimeter

Similar devices

Other devices filed under FDA product code GDI (Dissector, Surgical, General & Plastic Surgery).

Other devices from Purple Surgical International Limited

See all devices from Purple Surgical International Limited →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)