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Upsylon™ Y Mesh Kit

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Upsylon™ Y Mesh Kit FDA UDI
Generic Name
Pelvic organ prolapse surgical mesh, synthetic polymer FDA UDI
Device Name
Traditional Y Mesh Kit FDA UDI
Model / Reference
M0068318220 FDA UDI
Description
Traditional Y Mesh Kit FDA UDI

Identifiers

Primary DI / UDI-DI
08714729848103 FDA UDI
FDA Product Code
OHD FDA UDI
GMDN Term
Pelvic organ prolapse surgical mesh, synthetic polymer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pelvic organ prolapse surgical mesh, synthetic polymer

Upsylon™ Y Mesh Kit by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pelvic organ prolapse surgical mesh, synthetic polymer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 4868dbe2-a764-4815-b0bb-a0da7885f721 33 fields · synced May 30, 2026