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Deknatel IPN011359

by Teleflex Incorporated

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

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 Number04026704591428 UDI-DI Date16 Oct 2015ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Deknatel
Generic Name
Polyolefin/fluoropolymer suture, monofilament
Model / Ref / Catalog
IPN011359, D-7068K
Primary DI / UDI-DI
04026704591428
FDA Product Code
GAW
GMDN Term
Polyolefin/fluoropolymer suture, monofilament
Device Class
Class II
Regulation Number
878.5010
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe
Size
Length — 90 Centimeter

Related devices

Category: Polyolefin/fluoropolymer suture, monofilament

Other devices from Teleflex Incorporated

See all devices from Teleflex Incorporated →

Properties

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

Other properties (8)

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