Filamide

FDA UDI

Class II (US FDA UDI)

by Meril Endo Surgery Private Limited

Identity

Trade Name: FILAMIDE FDA UDI
Generic Name: Nylon suture, non-bioabsorbable, monofilament FDA UDI
Device Name: Non-absorbable Polyamide Surgical Suture FDA UDI
Model / Reference: NYL50698 FDA UDI
Description: Non-absorbable Polyamide Surgical Suture FDA UDI

Identifiers

Catalog Number: NYL50698 FDA UDI
Primary DI / UDI-DI: 18904255203164 FDA UDI
510(k) Number: K172149 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Nylon suture, non-bioabsorbable, monofilament

Filamide by Meril Endo Surgery Private Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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DemeLON — DemeTECH Corp · Class II
SUPRAMID — S. Jackson, Inc. · Class II
ETHILON — Ethicon Inc. · Class II
UNIFY Nylon Surgical Sutures — APPLIED DENTAL, INC. · Class II
DemeLON — DemeTECH Corp · Class II

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Meril Endo Surgery Private Limited

Sources (1)

FDA UDI b2d234d9-e67f-45b6-94f1-0565ae0eed21 37 fields · synced Jun 8, 2026