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Hunter

FDA UDI

Class II (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
HUNTER FDA UDI
Generic Name
Tendon sheath regeneration implant FDA UDI
Device Name
Hunter Active Tendon Implant BC FDA UDI
Model / Reference
ATBC2040 FDA UDI
Description
Hunter Active Tendon Implant BC FDA UDI

Identifiers

Catalog Number
ATBC2040 FDA UDI
Primary DI / UDI-DI
00840420186799 FDA UDI
FDA Product Code
HXA FDA UDI
GMDN Term
Tendon sheath regeneration implant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 20 Centimeter FDA UDI
Width — 4 Millimeter FDA UDI

Category: Tendon sheath regeneration implant

Hunter by Wright Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon sheath regeneration implant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wright Medical Technology, Inc.

Sources (1)

  • FDA UDI b2c16819-9329-4670-963e-dca2d4d8c778 36 fields · synced Jun 8, 2026