← Back to catalogue

Atramat

FDA UDI

Class II (US FDA UDI)

by Internacional Farmacéutica S.A DE C.V

Identity

Trade Name
ATRAMAT FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
ATRAMAT POLYESTER SURGICAL SUTURE GREEN USP 2-0 EP 3, 75 CM DOUBLE NEEDLE CVS-20 CARDIOVASCULAR PREMIUM TAPER POINT 20 MM 1/2 CIRCLE WITH PLEDGET POLIESTER USP 2-0, 75 CM DOBLE AGUJA CVS-20 CARDIOVASCULAR AHUSADA PREMIUM 20 MM 1/2 CIRCULO CON PLEDGET FDA UDI
Model / Reference
POLIESTER FDA UDI
Description
ATRAMAT POLYESTER SURGICAL SUTURE GREEN USP 2-0 EP 3, 75 CM DOUBLE NEEDLE CVS-20 CARDIOVASCULAR PREMIUM TAPER POINT 20 MM 1/2 CIRCLE WITH PLEDGET POLIESTER USP 2-0, 75 CM DOBLE AGUJA CVS-20 CARDIOVASCULAR AHUSADA PREMIUM 20 MM 1/2 CIRCULO CON PLEDGET FDA UDI

Identifiers

Catalog Number
CVS2052/2-75P FDA UDI
Primary DI / UDI-DI
07500142079856 FDA UDI
510(k) Number
K905285 FDA UDI
FDA Product Code
GAS FDA UDI
GMDN Term
Polyester suture, non-bioabsorbable, multifilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5000 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 20 Millimeter FDA UDI

Category: Polyester suture, non-bioabsorbable, multifilament

Atramat by Internacional Farmacéutica S.A DE C.V — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyester suture, non-bioabsorbable, multifilament.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d73a8392-a65f-442f-a69a-f161687952b8 39 fields · synced Jun 8, 2026