FDA UDI In Commercial Distribution 🇺🇸 United States

ADC®

DI: 00634782099060 · Model: 39800 · AMERICAN DIAGNOSTIC CORP
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ADC®
Primary DI
00634782099060
Version / Model
39800
Catalog Number
39800
Company Name
AMERICAN DIAGNOSTIC CORP
Labeler DUNS
108999095
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-11
Public Version
2
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
d9b917de-e9fe-4a9f-a0db-822b492cfbce

Device Description

PT Kit,

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KQW Goniometer, Nonpowered
GWZ Percussor

GMDN Terms

Code Name
33651 Manual goniometer
11950 Percussion hammer, manual, reusable

Identifiers

Type ID
Package 00634782600488
Primary 00634782099060

Customer Contacts