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Fssb

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
FSSB FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
2xVLZ-8.5-350 6/0 pe 45cm FDA UDI
Model / Reference
A013PEW FDA UDI
Description
2xVLZ-8.5-350 6/0 pe 45cm FDA UDI

Identifiers

Primary DI / UDI-DI
00848782032570 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

Fssb 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

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

Sources (1)

  • FDA UDI 989dbcd4-3a51-432d-b1d4-63205387ba0b 35 fields · synced Jun 6, 2026