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Pass Lp

FDA UDI

Class II (US FDA UDI)

by Medicrea International SA

Identity

Trade Name
PASS LP FDA UDI
Generic Name
Bone-screw internal spinal fixation system, sterile FDA UDI
Device Name
ROD Ø 5.5mm x 400mm FDA UDI
Model / Reference
B02125540S FDA UDI
Description
ROD Ø 5.5mm x 400mm FDA UDI

Identifiers

Primary DI / UDI-DI
03613720173229 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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: Bone-screw internal spinal fixation system, sterile

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

Similar devices

Also classified as Bone-screw internal spinal fixation system, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 71c378d0-ee45-4c89-a2dd-c44fae169c9c 33 fields · synced May 30, 2026