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Vascufil

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Vascufil FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, monofilament FDA UDI
Device Name
Coated Monofilament Polybutester,CV-22,D/A,1x Blue Strand FDA UDI
Model / Reference
88864741-21V FDA UDI
Description
Coated Monofilament Polybutester,CV-22,D/A,1x Blue Strand FDA UDI

Identifiers

Primary DI / UDI-DI
10884521102101 FDA UDI
510(k) Number
K990952 FDA UDI
FDA Product Code
GAT FDA UDI
GMDN Term
Polyester suture, non-bioabsorbable, monofilament 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 30 Inch FDA UDI

Category: Polyester suture, non-bioabsorbable, monofilament

Vascufil by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K990952 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 6490918d-1973-4eda-8a89-5a0ae4ece122 37 fields · synced May 30, 2026