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B-P Total Shoulder System

FDA UDI

Class II (US FDA UDI)

by Endotec, Inc.

Identity

Trade Name
B-P TOTAL SHOULDER SYSTEM FDA UDI
Generic Name
Total shoulder prosthesis FDA UDI
Device Name
B-P SHOULDER GLENOID BEARING SIZE 2, 2.5 MM THICKNESS, 48 MM HUMERAL HEAD FDA UDI
Model / Reference
02-02-2248 FDA UDI
Description
B-P SHOULDER GLENOID BEARING SIZE 2, 2.5 MM THICKNESS, 48 MM HUMERAL HEAD FDA UDI

Identifiers

Catalog Number
02-02-2248 FDA UDI
Primary DI / UDI-DI
00814193025098 FDA UDI
510(k) Number
K904879 FDA UDI
FDA Product Code
KWS FDA UDI
GMDN Term
Total shoulder prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 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

Dimensions & Sizes

Size
Width — 2.5 Millimeter FDA UDI
Outer Diameter — 48 Millimeter FDA UDI

Category: Total shoulder prosthesis

B-P Total Shoulder System by Endotec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total shoulder prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endotec, Inc.

Sources (1)

  • FDA UDI bddc2f53-dba7-42ba-b38c-0b425e6d4d39 37 fields · synced May 30, 2026