FDA UDI In Commercial Distribution 🇺🇸 United States

Artisential Fenestrated Forceps

DI: 08800042701000 · Model: AUF01-LV · LIVSMED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Artisential Fenestrated Forceps
Primary DI
08800042701000
Version / Model
AUF01-LV
Company Name
LIVSMED
Labeler DUNS
688360116
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-21
Public Version
1
Public Version Date
2024-01-29
Public Version Status
New
Public Device Record Key
eadb1585-967a-4c6b-94da-a141c9a88706

Device Description

Sterile Single-Use Tissue Manipulation Forceps

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
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
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
61839 Rigid endoscopic tissue manipulation forceps, single-use

Identifiers

Type ID
Primary 08800042701000

Customer Contacts

Phone
833-548-7633

Device Sizes

Type Value Unit Text
Shaft Length 38 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 50 Degrees Celsius