FDA UDI In Commercial Distribution 🇺🇸 United States

ReNew

DI: 00811099013976 · Model: 3232 · MICROLINE SURGICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
ReNew
Primary DI
00811099013976
Version / Model
3232
Catalog Number
3232
Company Name
MICROLINE SURGICAL, INC.
Labeler DUNS
184080570
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2020-01-13
Public Version
1
Public Version Date
2020-01-21
Public Version Status
New
Public Device Record Key
b688de46-24df-4eb4-8150-ed68ca5365f1

Device Description

Disposable Modified Traditional Grasper

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
No
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

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

Identifiers

Type ID
Primary 00811099013976
Unit of Use 00811099013945