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

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number07500142031953 UDI-DI	Date5 Jul 2018Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Atramat
Generic Name: Silk suture
Model / Ref / Catalog: SEDA, R3038

Primary DI / UDI-DI: 07500142031953
510(k) Number: K905287
FDA Product Code: GAP
GMDN Term: Silk suture

Device Class: Class II
Regulation Number: 878.5030
GUDID distribution status: In Commercial Distribution

Size: Length — 30 Millimeter

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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