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Verza Guidance System Master Carton 610-1500-MC

by Civco Medical Instruments Co., Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841436111706 UDI-DI Date22 Aug 2017ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Verza Guidance System Master Carton
Generic Name
Needle guide, single-use
Model / Ref / Catalog
610-1500-MC
Primary DI / UDI-DI
00841436111706
510(k) Number
FDA Product Code
ITX
GMDN Term
Needle guide, single-use
Device Class
Class II
Regulation Number
892.1570
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Ethylene Oxide
Size
Width — 1.32 Inch
Length — 1.05 Inch

Related devices

Cleared under the same submission (K160806)

Show all (12)

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No