FDA UDI In Commercial Distribution 🇺🇸 United States

Bovie

DI: 00887482181324 · Model: IDS-210 · ASPEN SURGICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Bovie
Primary DI
00887482181324
Version / Model
IDS-210
Company Name
ASPEN SURGICAL PRODUCTS, INC.
Labeler DUNS
027680821
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-26
Public Version
3
Public Version Date
2025-10-29
Public Version Status
Update
Public Device Record Key
eed0621d-a833-4466-b5c4-14e23158de54

Device Description

Bovie High Frequency Electrosurgical Generator

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 00887482181324

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 75 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius