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Mericron Xl

FDA UDI

Class II (US FDA UDI)

by Meril Endo Surgery Private Limited

Identity

Trade Name
MERICRON XL FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
Non absorbable Poly (Ethylene Terephthalate) Surgical Suture USP FDA UDI
Model / Reference
PXL01548GZ FDA UDI
Description
Non absorbable Poly (Ethylene Terephthalate) Surgical Suture USP FDA UDI

Identifiers

Catalog Number
PXL01548GZ FDA UDI
Primary DI / UDI-DI
18904255215242 FDA UDI
510(k) Number
K172149 FDA UDI
FDA Product Code
GAT 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

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
MRI Safety
MR Safe FDA UDI

Category: Polyester suture, non-bioabsorbable, multifilament

Mericron Xl by Meril Endo Surgery Private Limited — 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

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Manufacturer

Sources (1)

  • FDA UDI f3f95915-9d15-4043-83bc-74add62a8f1c 37 fields · synced Jun 8, 2026