FDA UDI In Commercial Distribution 🇺🇸 United States

superDimension

DI: 10884521200517 · Model: SDBF1000 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
superDimension
Primary DI
10884521200517
Version / Model
SDBF1000
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
7
Public Version Date
2022-04-08
Public Version Status
Update
Public Device Record Key
7a7cad72-a6e0-427e-8eb8-00166e3b39e6

Device Description

Pre-Marked Biopsy 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
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KNW INSTRUMENT, BIOPSY

GMDN Terms

Code Name
38711 Flexible endoscopic biopsy forceps, single-use

Identifiers

Type ID
Package 20884521200514
Primary 10884521200517

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry