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Alliant Biotech

FDA UDI

Class I (US FDA UDI)

by Medisurge

Identity

Trade Name
Alliant Biotech FDA UDI
Generic Name
Surgical saw blade, reciprocating, single-use FDA UDI
Device Name
3/4" Wide TK Saw Blade FDA UDI
Model / Reference
3/4" FDA UDI
Description
3/4" Wide TK Saw Blade FDA UDI

Identifiers

Catalog Number
WZ-1-5560 FDA UDI
Primary DI / UDI-DI
G611WZ155600 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, reciprocating, single-use 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

Yes

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: Surgical saw blade, reciprocating, single-use

Alliant Biotech by Medisurge — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, reciprocating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medisurge

Sources (1)

  • FDA UDI 75099749-c6cb-443f-9398-3b45aa15ea3d 35 fields · synced May 31, 2026