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Duckbee Basket Punch, medium Left curved shaft

FDA UDI

Class I (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name
Duckbee Basket Punch, medium Left curved shaft FDA UDI
Generic Name
Ligament reconstruction instrument set, reusable FDA UDI
Model / Reference
110048710 FDA UDI

Identifiers

Catalog Number
361110bsm FDA UDI
Primary DI / UDI-DI
10818674029787 FDA UDI
FDA Product Code
LXH 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ligament reconstruction instrument set, reusable

Duckbee Basket Punch, medium Left curved shaft 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

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Manufacturer

Manufacturer
T.a.g Medical Products Agricultural Cooperative Association

Sources (1)

  • FDA UDI bdc8bfdc-2685-49f7-8274-734b97ac88da 33 fields · synced May 30, 2026