← Back to catalogue

Ligapass

FDA UDI

Class II (US FDA UDI)

by Medicrea International SA

Identity

Trade Name
LIGAPASS FDA UDI
Generic Name
Internal orthopaedic fixation system, cerclage wire/cable, sterile FDA UDI
Device Name
LIGAPASS 2.0 CONNECTOR FDA UDI
Model / Reference
B08106005S FDA UDI
Description
LIGAPASS 2.0 CONNECTOR FDA UDI

Identifiers

Primary DI / UDI-DI
03613720191902 FDA UDI
510(k) Number
K132395 FDA UDI
FDA Product Code
OWI FDA UDI
GMDN Term
Internal orthopaedic fixation system, cerclage wire/cable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3010 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

Category: Internal orthopaedic fixation system, cerclage wire/cable, sterile

Ligapass by Medicrea International SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Internal orthopaedic fixation system, cerclage wire/cable, sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI ba62ee05-2b11-4785-9f43-f5d2652d2b60 34 fields · synced Jun 8, 2026