FDA UDI In Commercial Distribution 🇺🇸 United States

ULTRADRAPE 2

DI: 10855683006965 · Model: Ultrasound Guided Peripheral Intravenous Barrier and Securement Device · PARKER LABORATORIES INC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
ULTRADRAPE 2
Primary DI
10855683006965
Version / Model
Ultrasound Guided Peripheral Intravenous Barrier and Securement Device
Catalog Number
34-10
Company Name
PARKER LABORATORIES INC
Labeler DUNS
002449593
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2025-05-20
Public Version
1
Public Version Date
2025-05-28
Public Version Status
New
Public Device Record Key
f7cc50a9-6e8b-4d34-82f4-3667660033aa

Device Description

Ultrasound Guided Peripheral Intravenous Barrier and Securement Device 4.68 in x 2.63 in

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
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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KGX Tape And Bandage, Adhesive

GMDN Terms

Code Name
58301 Synthetic polymer semi-permeable film dressing, adhesive

Identifiers

Type ID
Package 20855683006962
Primary 10855683006965
Unit of Use 00855683006968

Customer Contacts

Phone
9732769500

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius