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Inhance Shoulder System

FDA UDI

Class I (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
INHANCE SHOULDER SYSTEM FDA UDI
Generic Name
Joint prosthesis implantation kit, single-use FDA UDI
Device Name
INHANCE SHOULDER SYSTEM GLENOID PREP KIT EXTRA SMALL NA FDA UDI
Model / Reference
7701-10-200 FDA UDI
Description
INHANCE SHOULDER SYSTEM GLENOID PREP KIT EXTRA SMALL NA FDA UDI

Identifiers

Catalog Number
770110200 FDA UDI
Primary DI / UDI-DI
10603295551881 FDA UDI
FDA Product Code
HWT FDA UDI
HTO FDA UDI
KIJ FDA UDI
GMDN Term
Joint prosthesis implantation kit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 FDA UDI
888.4540 FDA UDI
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Joint prosthesis implantation kit, single-use

Inhance Shoulder System by Depuy (ireland) — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Joint prosthesis implantation kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI bedb744c-fa1a-4cb1-81a4-8ac765f46e40 35 fields · synced May 30, 2026