FDA UDI In Commercial Distribution 🇺🇸 United States

Pocket Press

DI: 10860280002609 · Model: PKT21 · COMPRESS INNOVATIONS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3

Basic Information

Brand Name
Pocket Press
Primary DI
10860280002609
Version / Model
PKT21
Company Name
COMPRESS INNOVATIONS, LLC
Labeler DUNS
035534207
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2025-07-22
Public Version
1
Public Version Date
2025-07-30
Public Version Status
New
Public Device Record Key
9b4d7dcf-a9b5-4373-afe3-7209ec7609b7

Device Description

Post-CIED Implant Compression Bandage

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FQM Bandage, Elastic

GMDN Terms

Code Name
10284 Pressure bandage, non-latex, single-use

Identifiers

Type ID
Primary 10860280002609
Unit of Use 00860280002602

Customer Contacts

Phone
929-444-9115