← Back to catalogue

Samba Screw

FDA UDI

Class I (US FDA UDI)

by Orthofix US LLC

Identity

Trade Name
SAMBA SCREW FDA UDI
Generic Name
Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated, non-sterile FDA UDI
Device Name
PARALLEL GUIDE SET FDA UDI
Model / Reference
11-1109-FD7 FDA UDI
Description
PARALLEL GUIDE SET FDA UDI

Identifiers

Primary DI / UDI-DI
18257200122028 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated, non-sterile

Samba Screw by Orthofix US LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated, non-sterile.

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

Manufacturer
Orthofix US LLC

Sources (1)

  • FDA UDI 39161231-0b98-4689-a59e-5c6c599ea7bc 34 fields · synced Jun 8, 2026