FDA UDI In Commercial Distribution 🇺🇸 United States

Dynamic DIAGNOSTICS, INC

DI: 00851255007111 · Model: PEN41 · BIOPROTECH INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Dynamic DIAGNOSTICS, INC
Primary DI
00851255007111
Version / Model
PEN41
Company Name
BIOPROTECH INC.
Labeler DUNS
688460539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-12
Public Version
1
Public Version Date
2025-03-20
Public Version Status
New
Public Device Record Key
367bab44-74eb-4e0f-8714-b7931f844998

Device Description

Slim, Rocker, 2.5” Non-stick Ceramic or FEP Coated Blade, 10 Ft(3M) or 16 Ft(5M) Cable, Holster, Blister package

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
61869 Open-surgery electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Package 20851255007115
Primary 00851255007111
Package 10851255007118

Premarket Submissions

Submission Number Supplement Number
K092732 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius