FDA UDI In Commercial Distribution 🇺🇸 United States

AllPro

DI: 00813360021291 · Model: 402 (Latch Mandel) · TEAM TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AllPro
Primary DI
00813360021291
Version / Model
402 (Latch Mandel)
Catalog Number
402-F-144
Company Name
TEAM TECHNOLOGIES, INC.
Labeler DUNS
078550672
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-23
Public Version
1
Public Version Date
2022-08-01
Public Version Status
New
Public Device Record Key
2db2e257-2e50-4c33-9774-8b6ead3824d3

Device Description

Prophy Cup, Latch Mandrel, Rib & Web, Firm White

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
No

Product Codes

Code Name
EHK Cup, Prophylaxis

GMDN Terms

Code Name
46938 Dental polishing cup, single-use

Identifiers

Type ID
Primary 00813360021291