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VariLift-C CIC2-A750

by Wenzel Spine

VariLift-C CIC2-A750 is a Class I device made by Wenzel Spine, listed in FDA GUDID since 23 Dec 2019 (UDI-DI 00813210020825), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00813210020825 UDI-DI Date23 Dec 2019ListedStatusListed 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  • Withdrawn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
VariLift-C
Generic name
Assistive gripping/twisting tool, reusable
Model / reference
CIC2-A750
Primary DI / UDI-DI
00813210020825
FDA product code
LXH
GMDN term
Assistive gripping/twisting tool, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code LXH (Orthopedic Manual Surgical Instrument).

Other devices from Wenzel Spine

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Properties

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