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Parasmillie

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
PARASMILLIE FDA UDI
Generic Name
Surgical saw blade, sagittal, single-use FDA UDI
Device Name
PARASMILLIE GRAFT HANDLE FDA UDI
Model / Reference
C8900 FDA UDI
Description
PARASMILLIE GRAFT HANDLE FDA UDI

Identifiers

Catalog Number
C8900 FDA UDI
Primary DI / UDI-DI
10845854034484 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical saw blade, sagittal, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Category: Surgical saw blade, sagittal, single-use

Parasmillie by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI a8e54f8d-5b4a-467b-b093-77d07996b611 35 fields · synced Jun 1, 2026