FDA UDI Not in Commercial Distribution 🇺🇸 United States

MARYLAND DISSECTOR

DI: B09926952000 · Model: 2695-200 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MARYLAND DISSECTOR
Primary DI
B09926952000
Version / Model
2695-200
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-26
Public Version
6
Public Version Date
2018-09-21
Public Version Status
Update
Public Device Record Key
26f98ae3-972c-4b8a-89df-40940f11e75b
Distribution End Date
2018-09-21

Device Description

MARYLAND DISSECTOR CURVED

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
No
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, Dry Heat Sterilization

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
32684 Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary B09926952000

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Device Size Text, specify 34cm Shaft
Device Size Text, specify 3mm Jaw