FDA.report

ADC®

Primary DI
00634782501792
Brand
ADC®
Company
AMERICAN DIAGNOSTIC CORP
Model
3691
Catalog number
3691
Device description
Buck Hammer,
Published
2016-09-21
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
false

Related Records

Contact Domains

Product Codes

CodeName
GWZPercussor

Product Code Classifications

CodeDeviceSpecialtyClass
GWZPercussorNeurology1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00634782501792PackageGS110In Commercial Distribution
00634782801793PackageGS110In Commercial Distribution
00634782001803PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00634782501792006347825017926347825017920634782501792
00634782801793006347828017936347828017930634782801793
00634782001803006347820018036347820018030634782001803

GMDN Terms

TermDefinition
Percussion hammer, manualA hand-held manual instrument designed to be used by an examining physician to gently tap near a patient's joints to test reflexes (e.g., patellar, ankle reflexes). It consists of a handle and shaft typically made of stainless steel, and has a head that may be ring, wedge, or dome shaped and is made of a soft material (e.g., rubber or plastic). Some devices may be fitted with a spike, brush, or other detachable component at the proximal end that can be used for neurological examinations. This is a reusable device.

Sterilization Methods

Method

Contacts

PhoneEmail
1-800-232-2670info@adctoday.com

Regulatory Flags

DUNS number
108999095
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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