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Hunter

FDA UDI

Class I (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
HUNTER FDA UDI
Generic Name
Tendon sheath regeneration implant FDA UDI
Model / Reference
PT300000 FDA UDI

Identifiers

Catalog Number
PT300000 FDA UDI
Primary DI / UDI-DI
00840420132338 FDA UDI
FDA Product Code
HXR FDA UDI
GMDN Term
Tendon sheath regeneration implant FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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
Width — 3 Millimeter FDA UDI
Length — 25 Centimeter FDA UDI

Category: Tendon sheath regeneration implant

Hunter by Wright Medical Technology, Inc. — Class I — 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 2500678b-670a-4ed3-997b-783eb104b6ea 35 fields · synced Jun 8, 2026