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Weck 544234

by Teleflex Incorporated 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 2 Nov 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number14026704936882 UDI-DI Date20 Oct 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 2 Nov 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Weck
Generic Name
Ligation clip, synthetic polymer, non-bioabsorbable
Model / Ref / Catalog
544234
Primary DI / UDI-DI
14026704936882
510(k) Number
FDA Product Code
FZP
GMDN Term
Ligation clip, synthetic polymer, non-bioabsorbable
Device Class
Class II
Regulation Number
878.4300
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe
Size
Depth — 0.06 Inch
Width — 0.3 Inch
Length — 0.45 Inch

Related devices

Cleared under the same submission (K133202)

Show all (12)

Other devices from Teleflex Incorporated

See all devices from Teleflex Incorporated →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number

Other properties (9)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No