FDA UDI In Commercial Distribution 🇺🇸 United States

Acclarent

DI: B504GSGC070CRF0 · Model: GC070CRF · Provision
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Acclarent
Primary DI
B504GSGC070CRF0
Version / Model
GC070CRF
Company Name
Provision
Labeler DUNS
016889401
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-08
Public Version
1
Public Version Date
2022-08-16
Public Version Status
New
Public Device Record Key
28eff36d-22cf-4653-9ef6-206b23eb8d55

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
Yes
PM Exempt
Yes
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
KDC Instrument, Surgical, Disposable

GMDN Terms

Code Name
61813 Laparoscopic access cannula, reprocessed

Identifiers

Type ID
Primary B504GSGC070CRF0

Customer Contacts

Phone
541-508-7520