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Ambler Surgical

FDA UDI

Class II (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Orthopaedic joint/limb rongeur FDA UDI
Device Name
Sauerbruch-Stille rongeur, 11 3/4'', double-action, straight square shaped jaws, 20.0mm bite, spring handle FDA UDI
Model / Reference
Sauerbruch-Stille rongeur FDA UDI
Description
Sauerbruch-Stille rongeur, 11 3/4'', double-action, straight square shaped jaws, 20.0mm bite, spring handle FDA UDI

Identifiers

Catalog Number
75-827 FDA UDI
Primary DI / UDI-DI
00190660152819 FDA UDI
510(k) Number
K081651 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Orthopaedic joint/limb rongeur FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4840 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

No

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: Orthopaedic joint/limb rongeur

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

Similar devices

Also classified as Orthopaedic joint/limb rongeur.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d455d212-d9f5-42ac-9c20-c712354aebd1 36 fields · synced May 30, 2026