← Back to catalogue

Adler Instrument Company

FDA UDI

Class II (US FDA UDI)

by Adler, Inc.

Identity

Trade Name
Adler Instrument Company FDA UDI
Generic Name
Bone/joint surgical power tool motor, electric FDA UDI
Device Name
Micro Kerrison ceramic 8 in 2 mm 40 degree up FDA UDI
Model / Reference
ADRD4882 FDA UDI
Description
Micro Kerrison ceramic 8 in 2 mm 40 degree up FDA UDI

Identifiers

Primary DI / UDI-DI
00810123201815 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Bone/joint surgical power tool motor, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4840 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

Yes

FDA UDI

Serial Number

No

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

Adler Instrument Company by Adler, Inc. — 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

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

Manufacturer

Manufacturer
Adler, Inc.

Sources (1)

  • FDA UDI 22a7c6b9-7b5f-4ebd-be6f-c9bd9b5ffd0d 34 fields · synced Jun 6, 2026