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Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Surgical drill chuck FDA UDI
Device Name
Steinmann pin chuck, 4'', fully cannulated, includes chuck key FDA UDI
Model / Reference
Steinmann pin chuck FDA UDI
Description
Steinmann pin chuck, 4'', fully cannulated, includes chuck key FDA UDI

Identifiers

Catalog Number
43-790 FDA UDI
Primary DI / UDI-DI
00190660106188 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Surgical drill chuck 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical drill chuck

Ambler Surgical by Ambler Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill chuck.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d53f9858-8153-4e72-8757-8ff2e89ff6ea 35 fields · synced Jun 8, 2026