FDA UDI In Commercial Distribution 🇺🇸 United States

CURETTE MOLT #2HD HD S/E

DI: D928105102HD0 · Model: 10-5102HD · W.H. Holden, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CURETTE MOLT #2HD HD S/E
Primary DI
D928105102HD0
Version / Model
10-5102HD
Company Name
W.H. Holden, Inc.
Labeler DUNS
183854322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-10
Public Version
1
Public Version Date
2023-10-18
Public Version Status
New
Public Device Record Key
efec3cbd-935a-4e45-a620-134acac5309b

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
Yes
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
EKE CURETTE, OPERATIVE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary D928105102HD0