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EVSRF Procedure Pack VC-PP-EVSRF

by Venclose Inc

EVSRF Procedure Pack VC-PP-EVSRF is a general surgical procedure kit (FDA Class II; FDA product code LRO, General Surgery Tray) made by Venclose Inc, listed in FDA GUDID since 21 Jan 2018 (UDI-DI 10858254006364), 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 Number10858254006364 UDI-DI Date21 Jan 2018ListedStatusListed 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  • Withdrawn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
EVSRF Procedure Pack
Generic name
General surgical procedure kit, non-medicated, single-use
Model / reference
VC-PP-EVSRF
Primary DI / UDI-DI
10858254006364
FDA product code
LRO
GMDN term
General surgical procedure kit, non-medicated, single-use
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LRO (General Surgery Tray).

Other devices from Venclose Inc

See all devices from Venclose Inc →

Properties

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