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DynaClip

FDA UDI

Class II (US FDA UDI)

by Medshape, Inc.

Identity

Trade Name
DynaClip FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
DYNACLIP STAPLE, 18X20X20MM FDA UDI
Model / Reference
3000-00-182020 FDA UDI
Description
DYNACLIP STAPLE, 18X20X20MM FDA UDI

Identifiers

Primary DI / UDI-DI
M9703000001820200 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

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
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic bone staple, non-adjustable

DynaClip by Medshape, Inc. — 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
Medshape, Inc.

Sources (1)

  • FDA UDI c613e117-0752-439d-b65d-5898eeb94ab3 33 fields · synced Jun 8, 2026