FDA.reportPublic FDA data

V. Mueller

Primary DI
00724995306304
Brand
V. Mueller
Company
STERIS Deutschland GmbH
Model
NL3826
Catalog number
NL3826
Device description
V. Mueller MICROSURGERY BIOPSY FORCEPS STRAIGHT, CUP-SHAPED JAWS JAWS 1MM DIAMETER OVERALL LENGTH 7-1/4 inches 18.4CM
Published
2026-09-25
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
GZXINSTRUMENT, MICROSURGICAL

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GZXInstrument, MicrosurgicalNeurology1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10885403075285PreviousGS10
00724995306304PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1088540307528510885403075285
00724995306304007249953063047249953063040724995306304

GMDN Terms#

Term, Definition table
TermDefinition
Open-surgery biopsy forceps, reusableA hand-held manual surgical instrument designed to obtain soft-tissue biopsy specimens from an open surgical wound or from within/near a large natural orifice (e.g., vagina, rectum) for histopathological examination; it is not intended for endoscopic or catheterized access. It is a metallic forceps-like instrument with a distal mechanism designed to bite/punch the biopsy sample and hold it for extraction when the handles are squeezed together. It is not designed for cutting bone (i.e., not a rongeur). This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)548-4873xx@xx.xx

Regulatory Flags#

DUNS number
537625100
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00724995267742Snowden-Pencer8820108820102026-09-25
00724995267773Snowden-Pencer8821118821112026-09-25
00724995267780Snowden-Pencer8821238821232026-09-25
00724995267797Snowden-Pencer8821248821242026-09-25
00724995267803Snowden-Pencer8821288821282026-09-25
00724995267896Snowden-Pencer8824008824002026-09-25
00724995267902Snowden-Pencer8830108830102026-09-25
00724995267926Snowden-Pencer8830508830502026-09-25
00724995267940Snowden-Pencer8832008832002026-09-25
00724995267957Snowden-Pencer8832018832012026-09-25
00724995267995Snowden-Pencer8838628838622026-09-25
00724995268008Snowden-Pencer8838678838672026-09-25
00724995268015Snowden-Pencer8838738838732026-09-25
00724995268022Snowden-Pencer8838758838752026-09-25
00724995268039Snowden-Pencer8838768838762026-09-25
00724995268046Snowden-Pencer8838788838782026-09-25
00724995268312Snowden-Pencer8850508850502026-09-25
00724995268329Snowden-Pencer8850518850512026-09-25
00724995268336Snowden-Pencer8850528850522026-09-25
00724995268343Snowden-Pencer8850538850532026-09-25

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00724995275082V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995275099V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995275105V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995275112V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995275129V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995293581V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995293598V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995293604V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995293611V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995306281V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00724995306298V. MuellerSTERIS Deutschland GmbHGZX2026-09-25
00190776424121MillenniumAvalign Technologies, Inc.GZX2026-08-27
00190776420376MillenniumAvalign Technologies, Inc.GZX2026-08-25
00190776419134MillenniumAvalign Technologies, Inc.GZX2026-08-23
00190776427191MillenniumAvalign Technologies, Inc.GZX2026-08-21
00190776414672MillenniumAvalign Technologies, Inc.GZX2026-08-18
00190776408640MillenniumAvalign Technologies, Inc.GZX2026-08-03
00190776407407MillenniumAvalign Technologies, Inc.GZX2026-07-31
00190776407414MillenniumAvalign Technologies, Inc.GZX2026-07-31
00190776422271MillenniumAvalign Technologies, Inc.GZX2026-07-31
00190776407322MillenniumAvalign Technologies, Inc.GZX2026-07-28
00190776404093MillenniumAvalign Technologies, Inc.GZX2026-07-24
00190776404116MillenniumAvalign Technologies, Inc.GZX2026-07-24
00190776404123MillenniumAvalign Technologies, Inc.GZX2026-07-24
00190776404130MillenniumAvalign Technologies, Inc.GZX2026-07-24
00190776404086MillenniumAvalign Technologies, Inc.GZX2026-07-22
00190776400613MillenniumAvalign Technologies, Inc.GZX2026-07-21
00190776403386MillenniumAvalign Technologies, Inc.GZX2026-07-21
00650551006978PMT® SUCTION INSTRUMENTSPMT CORPORATIONGZX2026-07-20
00190776402099MillenniumAvalign Technologies, Inc.GZX2026-07-19