FDA UDI In Commercial Distribution 🇺🇸 United States

Tera

DI: 00810192476664 · Model: 20-10000071 · ACUITY SURGICAL DEVICES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tera
Primary DI
00810192476664
Version / Model
20-10000071
Catalog Number
20-10000071
Company Name
ACUITY SURGICAL DEVICES, LLC
Labeler DUNS
025855111
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-10
Public Version
1
Public Version Date
2026-02-18
Public Version Status
New
Public Device Record Key
9aa08cd6-2cd3-4f4b-a2bc-3fb3833be9ec

Device Description

TERA-T Retractor Driver Shaft

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
Yes
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

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00810192476664

Device Sizes

Type Value Unit Text
Length 162 Millimeter