Identity

Trade Name
DORO LUNA® Retractor System FDA UDI
Generic Name
Skull clamp FDA UDI
Device Name
DORO LUNA® Compact Retractor System & DORO® QR3 Skull Clamp consisting of: 3116-151 3116-141 3116-131 3116-121 3116-111 1201.091 1203.091 1201.006 1203.004 1203.003 1203.002 1203.001 1001.001 FDA UDI
Model / Reference
1203.210 FDA UDI
Description
DORO LUNA® Compact Retractor System & DORO® QR3 Skull Clamp consisting of: 3116-151 3116-141 3116-131 3116-121 3116-111 1201.091 1203.091 1201.006 1203.004 1203.003 1203.002 1203.001 1001.001 FDA UDI

Identifiers

Primary DI / UDI-DI
04250435519622 FDA UDI
510(k) Number
K001808 FDA UDI
FDA Product Code
HBL FDA UDI
GMDN Term
Skull clamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4460 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusableSurgical retractor/retraction system blade, reusableSkull clamp

DORO LUNA® Retractor System by pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Skull clamp.

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 551a582a-69fb-4ce6-b9d7-721a5c19856e 34 fields · synced Jun 8, 2026