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Fumedica

FDA UDI

Class II (US FDA UDI)

by Surgical Specialties México, S. de R.L. de C.V.

Identity

Trade Name
FUMEDICA FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
2xHRS-26-680P USP 2-0 Polyester 75 cm with Pledgets 3x6mm. sterile. 10pcs. x 2 green and 2 white per Box VA10.1 FDA UDI
Model / Reference
H26-2723N FDA UDI
Description
2xHRS-26-680P USP 2-0 Polyester 75 cm with Pledgets 3x6mm. sterile. 10pcs. x 2 green and 2 white per Box VA10.1 FDA UDI

Identifiers

Catalog Number
H26-2723N FDA UDI
Primary DI / UDI-DI
00848782042814 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

Category: Polyester suture, non-bioabsorbable, multifilament

Fumedica by Surgical Specialties México, S. de R.L. de C.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 29d1d82c-c2ae-4a9a-b75b-fdc5f23cc2a0 36 fields · synced Jun 8, 2026