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Joseph Bayonet Bone Saw

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
JOSEPH BAYONET BONE SAW FDA UDI
Generic Name
Manual surgical saw blade, rigid FDA UDI
Device Name
JOSEPH BAYONET BONE SAW SINGLE ENDED/SIDED LEFT HANDED BLADE FDA UDI
Model / Reference
345-256 FDA UDI
Description
JOSEPH BAYONET BONE SAW SINGLE ENDED/SIDED LEFT HANDED BLADE FDA UDI

Identifiers

Catalog Number
345-256 FDA UDI
Primary DI / UDI-DI
00192896078307 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Manual surgical saw blade, rigid FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 8 Inch FDA UDI

Category: Manual surgical saw blade, rigid

Joseph Bayonet Bone Saw by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual surgical saw blade, rigid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI e2bca22e-035d-425f-985e-e5994b212d72 36 fields · synced Jun 8, 2026