FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10193489181708 · Model: ERKSMOKE3002P · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
MEDLINE
Primary DI
10193489181708
Version / Model
ERKSMOKE3002P
Catalog Number
ERKSMOKE3002P
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-08
Public Version
1
Public Version Date
2025-01-16
Public Version Status
New
Public Device Record Key
97c4e889-1c1f-4b1d-8b7a-f2f83f692637

Device Description

PENCIL, CAUTERY, PTFE, SMOKE EVAC,ROCKER

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
47998 Surgical fluid/smoke waste management system

Identifiers

Type ID
Package 20193489181705
Primary 10193489181708

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a clean, cool and dry place. Handle with care to avoid damage to the packaging and its content during transportation and storage.