Elastic Staples

FDA UDI

Class II (US FDA UDI)

by Trimed, INC.

Identity

Trade Name: Elastic Staples FDA UDI
Generic Name: Orthopaedic bone staple, non-adjustable FDA UDI
Device Name: Nitinol Staple,10mm x 13/13mm FDA UDI
Model / Reference: ES-10x13 FDA UDI
Description: Nitinol Staple,10mm x 13/13mm FDA UDI

Identifiers

Catalog Number: ES-10x13 FDA UDI
Primary DI / UDI-DI: 00842188108969 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: Orthopaedic bone staple, non-adjustable

Elastic Staples by Trimed, INC. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Orthopaedic bone staple, non-adjustable.

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Arthrex® — Arthrex, Inc. · Class II
Speed Arc — Synthes · Class II
JAWS Nitinol Staple System — Paragon 28 · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Trimed, INC.

Sources (1)

FDA UDI 8c22ba5d-975b-40d4-ae39-51cf67d82d6d 35 fields · synced Jun 1, 2026