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Cross Links 50mm

FDA UDI

Class II (US FDA UDI)

by mahe medical gmbh

Identity

Trade Name
Cross Links 50mm FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
Cross Links 50mm FDA UDI
Model / Reference
SCC0120-0050 FDA UDI
Description
Cross Links 50mm FDA UDI

Identifiers

Catalog Number
SCC0120-0050 FDA UDI
Primary DI / UDI-DI
EMAHSCC012000500 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bone-screw internal spinal fixation system, non-sterile

Cross Links 50mm by mahe medical gmbh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
mahe medical gmbh

Sources (1)

  • FDA UDI 633d4c44-731e-436e-b865-92d4c22095b5 35 fields · synced Jun 1, 2026