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BC Reflex Uni

FDA UDI

Class II (US FDA UDI)

by Laboratoires Bodycad Inc

Identity

Trade Name
BC Reflex Uni FDA UDI
Generic Name
Unicondylar knee prosthesis FDA UDI
Model / Reference
018-001 FDA UDI

Identifiers

Catalog Number
018-001 FDA UDI
Primary DI / UDI-DI
00688346002072 FDA UDI
510(k) Number
K191996 FDA UDI
FDA Product Code
HSX FDA UDI
GMDN Term
Unicondylar knee prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3520 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Unicondylar knee prosthesis

BC Reflex Uni by Laboratoires Bodycad Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Unicondylar knee prosthesis.

Cleared under the same submission

K191996 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b126aab1-a0cf-4821-92a3-5ffa44d2fd19 34 fields · synced Jun 7, 2026