ADC®

Primary DI
00634782501815
Brand
ADC®
Company
AMERICAN DIAGNOSTIC CORP
Model
3695
Catalog number
3695
Device description
Wartenberg Pinwheel,
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

Contact Domains#

Product Codes#

Code, Name table
CodeName
GWYPinwheel
GWZPercussor

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GWYPinwheelNeurology1
GWZPercussorNeurology1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00634782501815PackageGS15In Commercial Distribution
00634782801816PackageGS110In Commercial Distribution
00634782001827PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00634782501815006347825018156347825018150634782501815
00634782801816006347828018166347828018160634782801816
00634782001827006347820018276347820018270634782001827

GMDN Terms#

Term, Definition table
TermDefinition
Pinwheel aesthesiometerA manual stimulator designed to determine tactile sensibility by testing a patient's discrimination of diameter in rods mounted on a disc. It typically consists of a disc, with protruding rods that differ in diameter, mounted on a rotary pin; the disc is manually rotated on the patient's skin by moving an integral handle at the proximal end. The rods may be sharply pointed for testing pain sensation. The device is typically used during physical examinations for detecting peripheral neuropathy and/or in diabetes mellitus or leprosy diagnostics. This is a reusable device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
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

Other Devices From This Company#

Primary DI, Brand, Model table
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00634782603045ADC54202542022026-03-31
00634782603052ADC54203542032026-03-31
00634782603069ADC54204542042026-03-31
00634782603076ADC54205542052026-03-31
00634782098384Adscope®603-04W603-04W2026-03-30
00634782100209Adscope®608-12COP608-12COP2026-03-30
00634782100216Adscope®608-12G608-12G2026-03-30
00634782100223Adscope®608-12I608-12I2026-03-30
00634782100230Adscope®608-12ST608-12ST2026-03-30
00634782100247Adscope®608-12MBK608-12MBK2026-03-30
00634782100254Adscope®608-12RGBK608-12RGBK2026-03-30
00634782100261Adscope®608-12RGW608-12RGW2026-03-30
00634782100834Adscope®608-12BK608-12BK2026-03-30
00634782101190Adscope®608-01MBK608-01MBK2026-03-30
00634782101299Adsoft®602-078BK1Q602-078BK1Q2026-03-30
00634782101305Adsoft®602-078PR1Q602-078PR1Q2026-03-30
00634782101312Adsoft®602-078TQ1Q602-078TQ1Q2026-03-30
00634782101329Adsoft®602-078G1Q602-078G1Q2026-03-30
00634782101336Adsoft®602-078Y1Q602-078Y1Q2026-03-30

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00817524029956J&J InstrumentsJ & J INSTRUMENTS INCGWY2023-06-08
00840183501389BR Surgical, LLCBR Surgical, LLCGWZ2023-03-28
00840183505318BR Surgical, LLCBR Surgical, LLCGWZ2023-03-28
00840183505394BR Surgical, LLCBR Surgical, LLCGWY2023-03-28
00840183506728BR Surgical, LLCBR Surgical, LLCGWZ2023-03-28
00840183507343BR Surgical, LLCBR Surgical, LLCGWZ2023-03-28
00840183508760BR Surgical, LLCBR Surgical, LLCGWZ2023-03-28
00840183519599BR Surgical, LLCBR Surgical, LLCGWZ2023-03-28
00634782099060ADC®AMERICAN DIAGNOSTIC CORPGWZ2023-01-11
10665973022786Tech-MedDukal LLCGWY2022-12-06
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00786511000240hammer RASHMAN CORPORATIONGWZ2022-12-02
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