FDA UDI Not in Commercial Distribution 🇺🇸 United States

PUNCH

DI: 00888118064806 · Model: 39-541-13-07 · KLS-Martin L.P.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PUNCH
Primary DI
00888118064806
Version / Model
39-541-13-07
Company Name
KLS-Martin L.P.
Labeler DUNS
826499238
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-26
Public Version
8
Public Version Date
2023-10-17
Public Version Status
Update
Public Device Record Key
86b8c0e0-4091-46cb-ac4c-dd608d93edbe
Distribution End Date
2021-04-20

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
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KBT PUNCH, TONSIL

GMDN Terms

Code Name
36199 ENT soft-tissue cutting forceps

Identifiers

Type ID
Primary 00888118064806

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 19 CM