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Speed

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
Speed FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
SPEED 11X15X13mm implant FDA UDI
Model / Reference
SE-111513 FDA UDI
Description
SPEED 11X15X13mm implant FDA UDI

Identifiers

Catalog Number
SE111513 FDA UDI
Primary DI / UDI-DI
00810633020135 FDA UDI
FDA Product Code
JDR FDA UDI
GMDN Term
Orthopaedic bone staple, non-adjustable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic bone staple, non-adjustable

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

Similar devices

Also classified as Orthopaedic bone staple, non-adjustable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI 069f19eb-c5fc-4294-a2c2-53c0501ea26a 36 fields · synced May 30, 2026