FDA UDI In Commercial Distribution 🇺🇸 United States

Dryswab

DI: 05060259070723 · Model: N/a · MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
125

Basic Information

Brand Name
Dryswab
Primary DI
05060259070723
Version / Model
N/a
Catalog Number
MW108
Company Name
MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED
Labeler DUNS
216096750
Distribution Status
In Commercial Distribution
Device Count in Pkg
125
Record Status
Published
Publish Date
2023-08-30
Public Version
1
Public Version Date
2023-09-07
Public Version Status
New
Public Device Record Key
2e7b46ca-795d-4826-a565-2b13af9e689d

Device Description

Dry Swab, Wood shaft with applicator, peel pouch, 1 swab

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
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
KXG Applicator, Absorbent Tipped, Sterile

GMDN Terms

Code Name
33722 General-purpose absorbent tip applicator/swab, single-use

Identifiers

Type ID
Package 25060259070727
Primary 05060259070723
Unit of Use 15060259070720

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
5 – 25 Degrees Celsius