← Back to catalogue

Betta Link FA Disposable Drill Bit Foot & Ankle

FDA UDI

Class I (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name
Betta Link FA Disposable Drill Bit Foot & Ankle FDA UDI
Generic Name
Ligament reconstruction instrument set, reusable FDA UDI
Model / Reference
110045589 FDA UDI

Identifiers

Catalog Number
183400bsm FDA UDI
Primary DI / UDI-DI
10818674026007 FDA UDI
FDA Product Code
HTO FDA UDI
GMDN Term
Ligament reconstruction instrument set, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ligament reconstruction instrument set, reusable

Betta Link FA Disposable Drill Bit Foot & Ankle by T.a.g Medical Products Agricultural Cooperative Association — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Ligament reconstruction instrument set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
T.a.g Medical Products Agricultural Cooperative Association

Sources (1)

  • FDA UDI 66a1aae4-cfa0-4db9-bb3a-81a918da0588 33 fields · synced Jun 1, 2026