FDA UDI In Commercial Distribution 🇺🇸 United States

Snowden-Pencer

DI: 10885403219986 · Model: 88-8347 · CAREFUSION 2200, INC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Snowden-Pencer
Primary DI
10885403219986
Version / Model
88-8347
Catalog Number
88-8347
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
7
Public Version Date
2024-02-02
Public Version Status
Update
Public Device Record Key
68e3554d-32dc-45ac-9dc5-4686d05b3d86

Device Description

Snowden-Pencer SLIDELOCK GRASPER MODULAR, DOUBLE ACTION 37CM, 5MM, 22MM JAW INSERT

Device Characteristics

Single Use
No
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
Yes
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HFI COAGULATOR, CULDOSCOPIC (AND ACCESSORIES)
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
35080 Rigid endoscopic tissue manipulation forceps, reusable

Identifiers

Type ID
Primary 10885403219986

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K151567 000
K925079 000