FDA UDI In Commercial Distribution 🇺🇸 United States

Sparrow Ascent

DI: 00850052017552 · Model: 313 · Spark Biomedical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sparrow Ascent
Primary DI
00850052017552
Version / Model
313
Catalog Number
313-k
Company Name
Spark Biomedical Inc.
Labeler DUNS
074715155
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-02
Public Version
1
Public Version Date
2026-02-10
Public Version Status
New
Public Device Record Key
ebdc3033-1e77-4940-934e-802eaf78f160

Device Description

Sparrow Ascent Kit - B2C (Mastoid Left 7)

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
PZR Percutaneous Nerve Stimulator For Opioid Withdrawal

GMDN Terms

Code Name
63321 Opioid withdrawal/irritable bowel symptom-relief periauricular nerve percutaneous electrical stimulator

Identifiers

Type ID
Primary 00850052017552