FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: B58210575310 · Model: 1057531 · GEORGE TIEMANN & CO.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
B58210575310
Version / Model
1057531
Catalog Number
1057531
Company Name
GEORGE TIEMANN & CO.
Labeler DUNS
107043630
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
1
Public Version Date
2020-10-02
Public Version Status
New
Public Device Record Key
6b44f20d-8374-4a9b-ade2-8d201260d057

Device Description

Curettes

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HTF CURETTE

GMDN Terms

Code Name
63259 Dermal curette

Identifiers

Type ID
Primary B58210575310

Customer Contacts

Phone
+1(631)273-0005 ext. 5223