Synapse

FDA UDI

Class I (US FDA UDI)

by Synthes

Identity

Trade Name: SYNAPSE FDA UDI
Generic Name: Bone holding forceps FDA UDI
Device Name: SYNAPSE COMPRESSION FORCEPS WITH SPEED NUT FDA UDI
Model / Reference: SD03.614.029 FDA UDI
Description: SYNAPSE COMPRESSION FORCEPS WITH SPEED NUT FDA UDI

Identifiers

Catalog Number: SD03614029 FDA UDI
Primary DI / UDI-DI: 10705034701592 FDA UDI
FDA Product Code: HTD FDA UDI
GMDN Term: Bone holding forceps FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone holding forceps

Synapse by Synthes — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone holding forceps.

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FORCEPS — KLS-Martin L.P. · Class I
Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
CLAMP — KLS-Martin L.P. · Class I
Novo Surgical — NOVO SURGICAL, INC. · Class I
Tecomet — Tecomet,Inc · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Synthes

Sources (1)

FDA UDI 0cde7102-60b9-45d8-b6d8-d3cc277bfc0d 35 fields · synced Jun 8, 2026