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Target Endoscopic Instrument

FDA UDI

Class I (US FDA UDI)

by SOLENDOS Inc.

Identity

Trade Name
Target Endoscopic Instrument FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
[Target] TMP0002 Micro Pituitary 2.0mm Up FDA UDI
Model / Reference
TMP0002 FDA UDI
Description
[Target] TMP0002 Micro Pituitary 2.0mm Up FDA UDI

Identifiers

Primary DI / UDI-DI
08800147701837 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Spinal rongeur 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: Spinal rongeur

Target Endoscopic Instrument by SOLENDOS Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SOLENDOS Inc.

Sources (1)

  • FDA UDI d851aac3-f8a3-488e-b264-4a3e15573005 34 fields · synced Jun 8, 2026