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Compress Device

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
Compress Device FDA UDI
Generic Name
Body femoral/tibial extension stem, coated FDA UDI
Model / Reference
178362 FDA UDI

Identifiers

Catalog Number
178362 FDA UDI
Primary DI / UDI-DI
00880304508965 FDA UDI
FDA Product Code
LZO FDA UDI
KWY FDA UDI
KRO FDA UDI
JDI FDA UDI
MEH FDA UDI
LPH FDA UDI
KWZ FDA UDI
JDC FDA UDI
KWS FDA UDI
MBF FDA UDI
KWT FDA UDI
GMDN Term
Body femoral/tibial extension stem, coated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3390 FDA UDI
888.3510 FDA UDI
888.3350 FDA UDI
888.3358 FDA UDI
888.3310 FDA UDI
888.3150 FDA UDI
888.3660 FDA UDI
888.3670 FDA UDI
888.3650 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

Category: Body femoral/tibial extension stem, coated

Compress Device by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body femoral/tibial extension stem, coated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Orthopedics, Inc.

Sources (1)

  • FDA UDI eeafdfa4-ac25-4afb-bd84-048d6c73158e 35 fields · synced May 30, 2026