FDA UDI In Commercial Distribution 🇺🇸 United States

Bovie

DI: 00887482149591 · Model: A821 · ASPEN SURGICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Bovie
Primary DI
00887482149591
Version / Model
A821
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
420f45ad-5782-4260-a921-0ccb402622ea

Device Description

Bipolar Forceps 8" Bayonet 2mm Tip

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
Yes
PM Exempt
No
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
47848 Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary 00887482149591

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8 Inch
Width 2 Millimeter