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Atramat Seda

by Internacional Farmacéutica S.A DE C.V 78 variants

Listed FDA GUDID listing, no authorization on record

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 Number07500142080494 UDI-DI Date27 Jul 2018ListedStatusListed GUDID: 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  • Withdrawn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
Atramat
Generic Name
Silk suture
Model / Ref / Catalog
SEDA, HPE1934-45
Primary DI / UDI-DI
07500142080494
510(k) Number
FDA Product Code
GAP
GMDN Term
Silk suture
Device Class
Class II
Regulation Number
878.5030
GUDID distribution status
In Commercial Distribution
Size
Length — 19 Millimeter

Related devices

Category: Silk suture

Cleared under the same submission (K905287)

Show all (12)

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No