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Expressew

FDA UDI

Class I (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
EXPRESSEW FDA UDI
Generic Name
Ligament reconstruction instrument set, single-use FDA UDI
Device Name
Expressew III AutoCapture+ Loading Tool/Retention Plate For use with E3AC+ Flexible Suture Passer FDA UDI
Model / Reference
288235 FDA UDI
Description
Expressew III AutoCapture+ Loading Tool/Retention Plate For use with E3AC+ Flexible Suture Passer FDA UDI

Identifiers

Catalog Number
288235 FDA UDI
Primary DI / UDI-DI
10886705027125 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Ligament reconstruction instrument set, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

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: Ligament reconstruction instrument set, single-use

Expressew by Medos International Sàrl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ligament reconstruction instrument set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medos International Sàrl

Sources (1)

  • FDA UDI d3bd51ac-c79c-45ca-9cac-4add04d6ec3e 35 fields · synced Jun 1, 2026