MetaFix™ BLP Locking Plate

FDA UDI

Class II (US FDA UDI)

by Merete GmbH

Identity

Trade Name: MetaFix™ BLP Locking Plate FDA UDI
Generic Name: Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Model / Reference: left 33 FDA UDI

Identifiers

Catalog Number: FH02033 FDA UDI
Primary DI / UDI-DI: 04048266040053 FDA UDI
FDA Product Code: KTT 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: Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

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Implantable

Yes

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Contains Latex

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Prescription Use

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Over-the-Counter

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Convenience Kit

FDA UDI

Combination Product

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HCT/P

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Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

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Serial Number

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Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Introducing MetaFix BLP Locking Plates, a non-bioabsorbable orthopedic fixation plate designed to stabilize traumatic/pathological fractures and fuse joints. Our flagship product is engineered with exceptional durability and safety in mind, featuring a firm implantation design and easy screw attachment. Whether you're treating a severe injury or managing chronic conditions, MetaFix BLP Locking Plates offer unparalleled support and stability.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Merete GmbH

Sources (1)

FDA UDI 36f0ce49-eb1c-4f17-8f5e-d1d7fba53bbd 36 fields · synced Jun 23, 2026