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Arrow®

FDA UDI

Class II (US FDA UDI)

by Fournitures Hospitalieres Industrie

Identity

Trade Name
ARROW® FDA UDI
Generic Name
Total reverse shoulder prosthesis FDA UDI
Model / Reference
265109 - CoCr CENTRED HUMERAL HEAD, Ø44 H16 FDA UDI

Identifiers

Primary DI / UDI-DI
03661489651090 FDA UDI
510(k) Number
K093599 FDA UDI
FDA Product Code
HSD FDA UDI
KWT FDA UDI
KWS FDA UDI
GMDN Term
Total reverse shoulder prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3650 FDA UDI
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

No

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

Yes

FDA UDI

Category: Total reverse shoulder prosthesis

Arrow® by Fournitures Hospitalieres Industrie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total reverse shoulder prosthesis.

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 199a4a1a-8dc1-47b3-a6b3-cdae04904223 33 fields · synced May 30, 2026