FDA UDI In Commercial Distribution 🇺🇸 United States

Kerrison sphenoid punch

DI: 04250676705471 · Model: 30-468-10 · Spiggle & Theis Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kerrison sphenoid punch
Primary DI
04250676705471
Version / Model
30-468-10
Catalog Number
30-468-10
Company Name
Spiggle & Theis Medizintechnik GmbH
Labeler DUNS
332893028
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-23
Public Version
1
Public Version Date
2022-10-03
Public Version Status
New
Public Device Record Key
abe91015-1ff9-4266-aba1-7639d18fd0c8

Device Description

90° upw., golden tip, totally detachable 1 mm, 18 cm

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
Yes
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
LRC INSTRUMENT, ENT MANUAL SURGICAL

GMDN Terms

Code Name
64337 Bone-coring punch, reusable

Identifiers

Type ID
Primary 04250676705471

Customer Contacts