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ASTRA DIRECTION INDICATOR SET LONG 24mm (16 PINS W/ PIN BLOCK)

FDA UDI

Class I (US FDA UDI)

by W.H. Holden, Inc.

Identity

Trade Name
ASTRA DIRECTION INDICATOR SET LONG 24mm (16 PINS W/ PIN BLOCK) FDA UDI
Generic Name
Surgical instrument/implant depth limiter, reusable FDA UDI
Model / Reference
10-7360L FDA UDI

Identifiers

Primary DI / UDI-DI
D928107360L0 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Surgical instrument/implant depth limiter, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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: Surgical instrument/implant depth limiter, reusable

ASTRA DIRECTION INDICATOR SET LONG 24mm (16 PINS W/ PIN BLOCK) by W.H. Holden, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/implant depth limiter, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W.H. Holden, Inc.

Sources (1)

  • FDA UDI 9d2c98ee-a7d6-42b3-8636-9f4382e0d112 32 fields · synced Jun 8, 2026