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LORRAINE 2.5/3.5mm Posterolateral Distal Humerus Plate, 11 Hole, Right

FDA UDIEUDAMED

Class II (US FDA UDI)

by Bonebridge AG

Identity

Trade Name
LORRAINE 2.5/3.5mm Posterolateral Distal Humerus Plate, 11 Hole, Right FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Model / Reference
B-162630 FDA UDI

Identifiers

Primary DI / UDI-DI
07640187462913 FDA UDI
510(k) Number
K250933 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

LORRAINE 2.5/3.5mm Posterolateral Distal Humerus Plate, 11 Hole, Right by Bonebridge AG — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bonebridge AG

Sources (2)

  • FDA UDI adfa6abf-be45-435d-8be6-91371189dff3 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026