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Multiloc

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
MULTILOC FDA UDI
Generic Name
Humerus intramedullary nail FDA UDI
Device Name
7MM TI MULTILOC HUMERAL NAIL RIGHT/CANN/195MM-STERILE FDA UDI
Model / Reference
04.016.195S FDA UDI
Description
7MM TI MULTILOC HUMERAL NAIL RIGHT/CANN/195MM-STERILE FDA UDI

Identifiers

Catalog Number
04016195S FDA UDI
Primary DI / UDI-DI
10886982089236 FDA UDI
510(k) Number
K120807 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Humerus intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Humerus intramedullary nail

Multiloc by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Humerus intramedullary nail.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI 38a3f747-c663-4bed-aa2a-c8cdba6d18fd 36 fields · synced May 30, 2026