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Megasorb

FDA UDI

Class II (US FDA UDI)

by Meril Endo Surgery Private Limited

Identity

Trade Name
MEGASORB FDA UDI
Generic Name
Polyglycolic acid suture FDA UDI
Device Name
Braided coated Polyglycolic Acid Surgical Suture USP FDA UDI
Model / Reference
PGA405637UZ FDA UDI
Description
Braided coated Polyglycolic Acid Surgical Suture USP FDA UDI

Identifiers

Catalog Number
PGA405637UZ FDA UDI
Primary DI / UDI-DI
18904255209876 FDA UDI
510(k) Number
K172659 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Polyglycolic acid suture FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4493 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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: Polyglycolic acid suture

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

Similar devices

Also classified as Polyglycolic acid suture.

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 2731b763-4675-4188-96b6-b131266f2580 37 fields · synced May 31, 2026