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Joseph Bone Saw

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
JOSEPH BONE SAW FDA UDI
Generic Name
Manual surgical saw, rigid FDA UDI
Device Name
JOSEPH BONE SAW SINGLE SIDED BLADE FDA UDI
Model / Reference
1100-466 FDA UDI
Description
JOSEPH BONE SAW SINGLE SIDED BLADE FDA UDI

Identifiers

Catalog Number
1100-466 FDA UDI
Primary DI / UDI-DI
00192896047631 FDA UDI
FDA Product Code
GDR FDA UDI
GMDN Term
Manual surgical saw, rigid 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

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 — 7.5 Inch FDA UDI

Category: Manual surgical saw, rigid

Joseph 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, rigid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5d5e6216-0143-4bd7-b4b4-ec50ed9e883e 36 fields · synced May 30, 2026