← Back to catalogue

Stryker 2000

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
STRYKER 2000 FDA UDI
Generic Name
Surgical saw blade, sagittal, single-use FDA UDI
Device Name
STRYKER 2000 SAGITTAL BLADE REPLACEMENT, ME-92 COATED 19.5 X 80 X 0.9MM (.035INCH) FDA UDI
Model / Reference
5072-195 FDA UDI
Description
STRYKER 2000 SAGITTAL BLADE REPLACEMENT, ME-92 COATED 19.5 X 80 X 0.9MM (.035INCH) FDA UDI

Identifiers

Catalog Number
5072-195 FDA UDI
Primary DI / UDI-DI
10845854000656 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, sagittal, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Dimensions & Sizes

Size
Height — 0.9 Millimeter FDA UDI
Length — 80 Millimeter FDA UDI
Width — 19.5 Millimeter FDA UDI
Height — 0.035 Inch FDA UDI

Stryker 2000 by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI f2ac28d0-5028-4fca-ae6a-089d78d4bad9 37 fields · synced May 31, 2026