FDA UDI In Commercial Distribution 🇺🇸 United States

WaterPAP™

DI: 10889483228708 · Model: WP-7700 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

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Basic Information

Brand Name
WaterPAP™
Primary DI
10889483228708
Version / Model
WP-7700
Catalog Number
WP-7700
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-15
Public Version
3
Public Version Date
2026-04-20
Public Version Status
Update
Public Device Record Key
913a92a2-1b7f-473f-8c56-8a626bdfb1dd

Device Description

WaterPAP™

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
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
BYE Attachment, Breathing, Positive End Expiratory Pressure

GMDN Terms

Code Name
46823 PEEP valve, single-use

Identifiers

Type ID
Primary 10889483228708
Previous 00709078013195
Package 20889483228705
Package 30889483228702

Customer Contacts