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Cellbrick Knee Spacer

FDA UDI

Class I (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
Cellbrick Knee Spacer FDA UDI
Generic Name
Orthopaedic cement spacer mould FDA UDI
Device Name
Tibial spacer mold, #3 FDA UDI
Model / Reference
9909-5430 FDA UDI
Description
Tibial spacer mold, #3 FDA UDI

Identifiers

Catalog Number
9909-5430 FDA UDI
Primary DI / UDI-DI
04719886906196 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic cement spacer mould FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic cement spacer mould

Cellbrick Knee Spacer by United Orthopedic Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic cement spacer mould.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
United Orthopedic Corp.

Sources (1)

  • FDA UDI db70780b-e82e-4044-bc2e-3ab373210545 35 fields · synced Jun 8, 2026