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Skimmer®

FDA UDI

Class I (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
Skimmer® FDA UDI
Generic Name
Surgical saw blade, oscillating, single-use FDA UDI
Device Name
BLADE 1882924HRE SKIMMER 27CM 2.9MM M4 FDA UDI
Model / Reference
1882924HRE FDA UDI
Description
BLADE 1882924HRE SKIMMER 27CM 2.9MM M4 FDA UDI

Identifiers

Primary DI / UDI-DI
00763000036744 FDA UDI
FDA Product Code
EQJ FDA UDI
GMDN Term
Surgical saw blade, oscillating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4140 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 27.0 Centimeter FDA UDI
Outer Diameter — 2.9 Millimeter FDA UDI
Angle — 15.0 degree FDA UDI

Category: Surgical saw blade, oscillating, single-use

Skimmer® by Medtronic Xomed, Inc. — 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
Medtronic Xomed, Inc.

Sources (1)

  • FDA UDI 0e922ad5-226a-4af1-a300-85c205e2ff03 35 fields · synced May 30, 2026