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Wire Saw

FDA UDI

Class I (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name
WIRE SAW FDA UDI
Generic Name
Manual surgical saw, flexible FDA UDI
Device Name
GIGLI FDA UDI
Model / Reference
24-600-30-07 FDA UDI
Description
GIGLI FDA UDI

Identifiers

Primary DI / UDI-DI
00888118033352 FDA UDI
FDA Product Code
GDR FDA UDI
GMDN Term
Manual surgical saw, flexible 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Manual surgical saw, flexible

Wire Saw by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual surgical saw, flexible.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KLS-Martin L.P.

Sources (1)

  • FDA UDI 0f5ec486-cbfa-4149-9bd7-7309bd844ad5 35 fields · synced Jun 8, 2026