FDA UDI In Commercial Distribution 🇺🇸 United States

PremierPro

DI: 00811220032371 · Model: 3772 · PRESTIGE AMERITECH, LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PremierPro
Primary DI
00811220032371
Version / Model
3772
Catalog Number
3772
Company Name
PRESTIGE AMERITECH, LTD.
Labeler DUNS
199692794
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-26
Public Version
2
Public Version Date
2026-03-23
Public Version Status
Update
Public Device Record Key
0fb44325-2370-4efa-9f3e-5f47a0e2e258

Device Description

Hose Adapter, Air Supply Pump REMUV, 6 ea/case

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FMR Device, Transfer, Patient, Manual

GMDN Terms

Code Name
46148 Patient transfer system, manual

Identifiers

Type ID
Primary 00811220032371

Customer Contacts

Phone
855-531-7699

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 158 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
10 – 70 Percent (%) Relative Humidity