Skip to content

V. Mueller OP0918-851

by Steris Corporation

V. Mueller OP0918-851 (OP0918851) is a Class I device made by Steris Corporation, listed in FDA GUDID since 5 Sep 2018 (UDI-DI 10885403094866), 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 Number10885403094866 UDI-DI Date5 Sep 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  • Withdrawn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
V. Mueller
Generic name
Lacrimal intubation set
Model / Ref / Catalog
OP0918-851, OP0918851
Primary DI / UDI-DI
10885403094866
FDA product code
HNL
GMDN term
Lacrimal intubation set
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Lacrimal intubation set

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)