FDA UDI In Commercial Distribution 🇺🇸 United States

Trauma Pad - Compress - 5"x 9"

DI: 00766588314198 · Model: R231-419 · Certified Safety Manufacturing, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trauma Pad - Compress - 5"x 9"
Primary DI
00766588314198
Version / Model
R231-419
Catalog Number
R231-419
Company Name
Certified Safety Manufacturing, Inc.
Labeler DUNS
788460483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-27
Public Version
1
Public Version Date
2023-02-06
Public Version Status
New
Public Device Record Key
5e314377-6c74-404a-8f10-5e5f2e946e55

Device Description

Trauma Pad - Compress - 5"x 9"

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EFQ GAUZE/SPONGE, INTERNAL

GMDN Terms

Code Name
46854 Wound-nonadherent dressing, absorbent, non-antimicrobial

Identifiers

Type ID
Primary 00766588314198

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K940348 000