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RemB

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
RemB FDA UDI
Generic Name
Bone/joint surgical power tool motor, electric FDA UDI
Device Name
Electric Reciprocating Saw FDA UDI
Model / Reference
6400037000 FDA UDI
Description
Electric Reciprocating Saw FDA UDI

Identifiers

Catalog Number
6400-037-000 FDA UDI
Primary DI / UDI-DI
07613154938339 FDA UDI
FDA Product Code
ERL FDA UDI
GMDN Term
Bone/joint surgical power tool motor, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone/joint surgical power tool motor, electric

RemB by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone/joint surgical power tool motor, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 6f38bb78-3630-4acd-97ee-ea9a344e582f 36 fields · synced Jun 6, 2026