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Havel's

FDA UDI

Class II (US FDA UDI)

by Havel's Incorporated

Identity

Trade Name
HAVEL'S FDA UDI
Generic Name
Nylon suture, non-bioabsorbable, monofilament FDA UDI
Device Name
SUTURE 5-0 NYLON 18"/DS-16 PROME FDA UDI
Model / Reference
SUT 5-0 NYLON 18"/DS-16 PROME FDA UDI
Description
SUTURE 5-0 NYLON 18"/DS-16 PROME FDA UDI

Identifiers

Catalog Number
BN65C FDA UDI
Primary DI / UDI-DI
B070BN65C0 FDA UDI
FDA Product Code
GAR FDA UDI
GMDN Term
Nylon suture, non-bioabsorbable, monofilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5020 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

Yes

FDA UDI

Category: Nylon suture, non-bioabsorbable, monofilament

Havel's by Havel's Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d9e082dd-bb8d-4111-aa1c-8254bef5d976 35 fields · synced May 29, 2026