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MicroAire®

FDA UDI

Class I (US FDA UDI)

by MicroAire Surgical Instruments LLC

Identity

Trade Name
MicroAire® FDA UDI
Generic Name
Surgical saw blade, oscillating, single-use FDA UDI
Device Name
LARGE OSC. SAW BLADE, 25.4mm x 90mm x 1.37mm FDA UDI
Model / Reference
ZO-7163 FDA UDI
Description
LARGE OSC. SAW BLADE, 25.4mm x 90mm x 1.37mm FDA UDI

Identifiers

Primary DI / UDI-DI
00847399013880 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Surgical saw blade, oscillating, single-use 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 25.4 Millimeter FDA UDI
Length — 90 Millimeter FDA UDI

Category: Surgical saw blade, oscillating, single-use

MicroAire® by MicroAire Surgical Instruments LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MicroAire Surgical Instruments LLC

Sources (1)

  • FDA UDI 00c7b19e-c277-4b72-a5ad-ffb2e738580c 34 fields · synced Jun 9, 2026