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G7®

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
G7® FDA UDI
Generic Name
Femoral head prosthesis trial FDA UDI
Model / Reference
010002501 FDA UDI

Identifiers

Catalog Number
010002501 FDA UDI
Primary DI / UDI-DI
00887868460524 FDA UDI
510(k) Number
K121874 FDA UDI
FDA Product Code
LPH FDA UDI
OQH FDA UDI
OQG FDA UDI
JDI FDA UDI
OQI FDA UDI
LWZ FDA UDI
PBI FDA UDI
KWZ FDA UDI
LZO FDA UDI
GMDN Term
Femoral head prosthesis trial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3350 FDA UDI
888.3353 FDA UDI
888.3310 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Femoral head prosthesis trial

G7® by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral head prosthesis trial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8ab19c43-954b-47ae-88e1-36940947f9b1 36 fields · synced May 30, 2026