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Pin, 3.0mm, DynaClip Staple, 3.0mm

FDA UDI

Class II (US FDA UDI)

by Medshape, Inc.

Identity

Trade Name
Pin, 3.0mm, DynaClip Staple, 3.0mm FDA UDI
Generic Name
Orthopaedic bone-fragment manipulator, single-use FDA UDI
Model / Reference
ED-10801-030 FDA UDI

Identifiers

Primary DI / UDI-DI
M970ED108010300 FDA UDI
FDA Product Code
HTY FDA UDI
GMDN Term
Orthopaedic bone-fragment manipulator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

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: Orthopaedic bone-fragment manipulator, single-use

Pin, 3.0mm, DynaClip Staple, 3.0mm by Medshape, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone-fragment manipulator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medshape, Inc.

Sources (1)

  • FDA UDI 490f57c2-9d2c-4a0f-a95d-a00b247e3afb 32 fields · synced Jun 8, 2026